Thermo Scientific GENESYS 30, GENESYS 50, GENESYS 180, GENESYS 40, GENESYS 140 Instruction Manual

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UV-Visible
GENESYS Family Spectrophotometers
User Guide
269-331300 Revision A February 2018
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© 2018 Thermo Fisher Scientific Inc. All rights reserved.
Eppendorf and UVette are either trademarks or registred trademarks of Eppendorf AG aktiengesellschaft. BrandTech is a trademark of BrandTech Scientific, Inc. Beckman is a trademark of BECKMAN COULTER, INC. All other trademarks are the property of Thermo Fisher Scientific Inc. and its subsidiaries.
For technical support, please contact: www.thermofisher.com
Thermo Fisher Scientific Inc. provides this document to its customers with a product purchase to use in the product operation. This document is copyright protected and any reproduction of the whole or any part of this document is strictly prohibited, except with the written authorization of Thermo Fisher Scientific Inc.
The contents of this document are subject to change without notice. All technical information in this document is for reference purposes only. System configurations and specifications in this document supersede all previous information received by the purchaser.
Thermo Fisher Scientific Inc. makes no representations that this document is complete, accurate or error­free and assumes no responsibility and will not be liable for any errors, omissions, damage or loss that might result from any use of this document, even if the information in the document is followed properly.
This document is not part of any sales contract between Thermo Fisher Scientific Inc. and a purchaser. This document shall in no way govern or modify any Terms and Conditions of Sale, which Terms and Conditions of Sale shall govern all conflicting information between the two documents.
For Research Use Only. This instrument or accessory is not a medical device and is not intended to be used for the prevention, diagnosis, treatment or cure of disease.
WARNING Avoid an explosion or fire hazard. This instrument or accessory is not designed for use in an explosive atmosphere.
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Contents

Chapter 1 GENESYS Spectrophotometers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Site Preparation and Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Operating Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Spectrophotometer Basics - GENESYS 40 and GENESYS 50. . . . . . . . . . . . . . . 3
Sample Compartment - GENESYS 40 and GENESYS 50 . . . . . . . . . . . . . . . 3
Single Cell Holder - GENESYS 40 and GENESYS 50 . . . . . . . . . . . . . . . . . . 4
Optional Sample Holders - GENESYS 40 and 50. . . . . . . . . . . . . . . . . . . . . . 5
Cell Holder Replacement - GENESYS 40 and 50 . . . . . . . . . . . . . . . . . . . . . . 6
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180
and BioMate 160. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Sample Compartment - GENESYS 140, GENESYS 150, GENESYS 180
& BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Single Cell Holder - GENESYS 140, GENESYS 150, GENESYS 180 &
BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Optional Single Sample Holders - GENESYS 140, GENESYS 150,
GENESYS 180 and BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Disposable 50 mL Microcell Holder – GENESYS 140, GENESYS 150,
GENESYS 180 and BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Beckman Cell Holder – GENESYS 140, GENESYS 150,
GENESYS 180 and BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Peltier Thermostatted Single Cell Holder – GENESYS 140,
GENESYS 150, GENESYS 180 and BioMate 160 . . . . . . . . . . . . . . . . . . 11
Sipper Accessory - GENESYS 140, GENESYS 150, GENESYS 180
and BioMate 160 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Fiber Optic Coupler and Probe (UV Vis systems only) . . . . . . . . . . . . . . . . . 21
Spectrophotometer Basics – All Models. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Halogen Lamp. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Lid Removal and Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Chapter 2 GENESYS On-board Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .33
GENESYS On-board Software Home Screen and Navigation. . . . . . . . . . . . 33
Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
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Viewing Saved Experiment Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Application Home. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Creating A New Method . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Experiment Execution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Data Analysis and Actions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Live Display Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Fixed Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Scan Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Quant Application. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Calibrated and Uncalibrated Quant Methods . . . . . . . . . . . . . . . . . . . . . . . . 47
Cell Changer Setup in Quant . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
C-Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Kinetics Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Importing Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Exporting Data and Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Performance Verification Tests and Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Running Performance Verification Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Customized Performance Verification Tests . . . . . . . . . . . . . . . . . . . . . . . . . 54
Customizing Stray Light Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Customizing Wavelength Accuracy Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Customizing Photometric Accuracy Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Accessory Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Cell Changer Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Sipper Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Calibrated Sipper. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Calibrating the Sipper . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Custom Workflows . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Peltier Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
Accessory Configuration in Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
SmartStart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Configuring and Switching to SmartStart Mode . . . . . . . . . . . . . . . . . . . . . . 75
Exiting SmartStart Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Connecting to VISIONlite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Enable the VISIONlite Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Printer Setup and Wi-Fi Printing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Setting Up USB Printer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Setting Up Thermal Printer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Configuring Network Paths. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
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Contents
Chapter 4 BioMate 160 Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .87
OD600 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
dsDNA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
RNA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
Protein BCA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
Protein Bradford . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Protein Lowry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
Protein Pierce 660 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
Protein Rapid Gold BCA. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
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GENESYS Spectrophotometers

This user guide applies to the following spectrophotometers:
• Intermediate capability models – the Thermo Scientific™ GENESYS™ 50 platform – with sample compartments configured for single samples only:
GENESYS™ 40 Vis
GENESYS 50 UV-Vis
• Advanced capability models – the GENESYS™ 150 platform – with sample compartments configured for:
–single samples
multi-cell changer option
Peltier thermostatted cell holder option
fiber optic probe option
• GENESYS™ 140 Vis
• GENESYS 150 UV-Vis
• GENESYS™ 180 UV-Vis
•BioMate™ 160
Note There is also a GENESYS™ 30 Vis that shares the sample compartment configuration of the GENESYS 50 platform but offers a user experience with a tactile rubber keypad, high resolution non-touch color 5-inch screen and simplified software. The GENESYS 30 has a separate dedicated user guide
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GENESYS Spectrophotometers

Considerations

Considerations
This document uses the following conditions:
DANGER Indicates a hazardous situation which, if not avoided, will result in death or serious injury.
WARNING Indicates a hazardous situation which, if not avoided, could result in death or serious injury.
CAUTION Indicates a hazardous situation which, if not avoided, could result in minor or moderate injury.
NOTICE Follow instructions with this label to avoid damaging the system hardware or losing data.
Note Contains helpful supplementary information.

Site Preparation and Safety

Before using the system, read the site preparation and safety manual on the documentation media provided. Always follow the safety precautions in that manual and in this document when using the system.

Operating Precautions

WARNING Do not operate this system without following the safety precautions described
in this manual and the documentation that came with your system.
The spectrophotometer contains precise optical components. Handle it carefully and follow these precautions.
• Do not allow moisture to leak into the instrument interior
• Wipe off spilled chemicals immediately
• Do not drop the instrument
• Protect the instrument from mechanical shock
• Protect the instrument from dust
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Lift here
Closure magnet
Light beam path
Detector lens
Monochromator window
Tray alignment posts
Drain
GENESYS Spectrophotometers

Spectrophotometer Basics - GENESYS 40 and GENESYS 50

Spectrophotometer Basics - GENESYS 40 and GENESYS 50
Remove all tape from the exterior of the instrument and inside the sample compartment.

Sample Compartment - GENESYS 40 and GENESYS 50

Thermo Scientific GENEYS Family Spectrophotometers 3
High durability constant torque hinges hold the lid at any angle
Window and lens protect interior optics from spills and vapors.
Magnet at front holds lid closed to exclude light when door is lowered
Sample holder tray aligns to posts on baseplate.
Excess spills drain to benchtop.
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Locater pin
Magnets
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 40 and GENESYS 50

Single Cell Holder - GENESYS 40 and GENESYS 50

Standard 10 mm cuvette holder Underside of a single cell holder
Tray features
• Able to contain spills up to 150 mL
• Can be removed by pulling up on the cell holder
• Can be washed in the sink or a dishwasher - dry promptly!
NOTICE
• Clean the tray with water and mild detergent. Ethanol and iso-propyl alcohol can be used if necessary but do not soak the tray in alcohols.
• Do not allow acetone, chlorocarbons or other aggressive organic solvents to contact the tray. The PC-ABS plastic will soften and discolor.
Removal – grasp cell holder and lift up and forward
Insertion – allow front magnet to engage. Lower cell holder into place, allowing back magnet to guide and engage
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Optional Sample Holders - GENESYS 40 and 50

Cell holder trays equipped to position other kinds of cells and samples are available. They insert and remove in the same way as the standard cell holder.
Te st tu b e h o ld e r
Tall test tube adapter
1
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 40 and GENESYS 50
Long path rectangular cell holder
Long path cylindrical cell holder
Filter holder
Accessory kit for hose entry/exit
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Lift here to open
Lid hold-down magnet
GENESYS Spectrophotometers

Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Cell Holder Replacement - GENESYS 40 and 50

Thermostatted cell holder and Adjustable filter holder accessories are supplied without a tray.
Loosen the captive screw at the base of the cell holder to remove it. Attach the new sample holder in the same way.
Note The Accessory Kit for Hose Entry/Exit is required to support use of the thermostatted cell holder. See Lid Removal and Replacement for additional installation instructions.
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Remove all tape from the exterior of the instrument and inside the sample compartment.

Sample Compartment - GENESYS 140, GENESYS 150, GENESYS 180 & BioMate 160

High durability constant torque hinges hold the lid at any angle
Magnet at front holds lid closed to exclude light when door is lowered
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Alignment posts
Opto-sensor
Drain
Detector lens
Monochromator window
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Align arrow on sample holder base with arrow on sample compartment and groove on sample compartment wall.
Window and lens protect interior optics from spills and vapors.
Sample holder aligns to posts on baseplate and groove.
Excess spills drain to benchtop. Opto-sensor is used for positioning cell changer.
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Locater pin
Ring magnet
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Single Cell Holder - GENESYS 140, GENESYS 150, GENESYS 180 & BioMate 160

Standard 10 mm cuvette holder
NOTICE
• Clean cell holders by wiping with a solution of mild detergent. Ethanol and isopropyl alcohol can be used if necessary but do not submerge the cell holder in liquid.
• Do not allow acetone, chlorocarbons or other aggressive organic solvents to contact the cell holder or base. The PC-ABS plastic will soften and discolor.
Removal—grasp blue knob and lift straight upInsertion—align arrow on left side of sample
compartment with arrow on sample holder accessory. Lower cell holder into place. Magnet holds accessory down. Pin under accessory base aligns cell holder in beam and prevents rotation.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Optional Single Sample Holders - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Cell holder trays equipped to position other kinds of cells and samples are available. They insert and remove in the same way as the standard cell holder.
Long path rectangular cell holder
Long path cylindrical cell holder
Filter holder
Disposable 50 μL Microcell Holder
Beckman cell holder
Peltier Thermostatted cell holder
Note Water thermostatted cell holders are not supported on this platform. See the Peltier Thermostatted Cell Holder accessory.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Disposable 50 mL Microcell Holder – GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Disposable plastic microcells with 50 μL chambers located at a Z-height of 8.5 mm and centered on the cell are supported by this accessory. At time of writing of this user guide, the Eppendorf™ UVette™ is the only brand supported, but see the insert with the accessory for updates. Cuvettes made by BrandTech™ are not supported because of poor manufacturing reproducibility in these cells.
Note Plastic microcells are not as transparent as quartz, especially at very short wavelengths. The combination of absorption by the cell and masking of the spectrophotometer beam required to restrict it to the 2.5 mm tall cell window reduces the energy passing through these cells. Photometric performance will be lower with these cells than with full size quartz cells.

Beckman Cell Holder – GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Beckman™ pioneered the use of a special type of microcell with volumes of 100 μL or less. These very short cells require a special holder to accommodate them at the appropriate Z-height for the cell and to mask off part of the spectrophotometer beam to ensure that light only passes though the sample, and not over it.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Peltier Thermostatted Single Cell Holder – GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

The accessory holds a single cell at a temperature between 20° and 60 °C with a precision of ≤0.2 °C and an absolute accuracy of ±0.5 °C.
Note The specification for absolute accuracy is limited by the accuracy of the thermocouple used in construction of the device. ±0.3° C is the specification of a superior quality thermocouple. Beyond this specification the cost of the thermocouple becomes exponentially higher and use of a calibrated thermocouple becomes a necessity if exceptionally high accuracy is a requirement.
In our tests, using a calibrated thermocouple probe, we generally find the temperature of the solution in the cuvette to fall within ±0.3 °C of the programmed absolute temperature.
The temperature measured and reported by the device is the temperature of the metal cell-holder block. The temperature of stirred liquid in a full size quartz cell will reach the same temperature as the cell holder block after approximately 6 minutes when heating from 23 °C to 35 °C. This is only a guide. Performance will vary if:
• The initial temperature is different
• The final temperature is below room temperature
• The cuvette is not stirred
• The cuvette is not made of glass or quartz
• The cuvette is a micro-cuvette
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
The experimental parameters for controlling the Peltier thermostatted cell holder include an equilibration time. This is a “wait time” between when the cell holder block reaches the target temperature and when the absorbance measurement is made. We strongly recommend that you place the probe of a digital thermometer or thermocouple of sufficient accuracy and precision in the liquid in a cell under what will be normal experimental conditions, and bring a quantity of appropriate matrix (solvent or buffer) to temperature in the cell holder while monitoring the temperature to determine performance under your experimental conditions. A white paper describing important considerations and limitations in thermostatting experiments is included with this documentation set. Refer to Introduction to Temperature Control for additional details.
In brief, however:
• Quartz conducts heat six times faster than plastic – samples in quartz cells come to temperature much faster than they do in plastic cells.
• A full size cell takes approximately 66% more time to reach equilibrium temperature if it is not stirred.
Installing the Accessory
Align white arrows as shown.
• Liquid in unstirred plastic cells did not heat to within 0.6 °C of the cell holder block temperature when heating in our experiments.
• Plastic microcells and semi-microcells have significantly reduced surface contact with the walls of the cell holder block compared to full size plastic cells or glass/quartz reduced volume cells. If using a reduced volume plastic cell it is essential that you perform some experiments to determine the appropriate equilibration time setting.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Lower the cell holder into the sample compartment so that the V engages with the groove on the side of the sample compartment and the hold-down magnet engages
Connect cables as shown.
• The power supply is identical to the instrument power supply
• Operate this accessory with the sample compartment lid open
• Do not close the sample compartment lid while the accessory is running
• Optional – the sample compartment lid can be removed while using this accessory
See “Peltier Configuration” on page 69 of this guide for instructions on configuring your method to use this accessory.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Sipper Accessory - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160

Introduction to Sipper Use
A detailed introduction to sippers and how they can be used to get the best results in different situations is provided in a separate document (English language only) included in the documentation media with this user guide.
Components of the Sipper System
Complete sipper systems come with the following components
Item Photograph
Sipper pump
Sample compartment insert with gooseneck
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Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
3 m PTFE transfer tubing
1 Flow cell, 160 µL volume with screw connector set
Smaller volume flow cells are available but the smaller window size cuts off some of the spec­trophotometer beam, reducing photometric performance. If the absorbance values measured are below 1.0, however, this will not make a noticeable impact on data quality.
Connector package
The connectors supplied are designed for use with the # 16 tubing supplied. They can also be used with smaller # 14 tubing with extra effort. To use larger # 25 tubing please purchase a larger connector separately.
Item Photograph
30 cm Silicone pump tubing (#16 size – 1.6 mm wall,
1.6 mm inside diameter)
1
GENESYS Spectrophotometers
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Inlet marker
Attach long connector to inlet
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Compatibility of the GENESYS Sipper with tubing sold by us for use with spectrophotometer sippers.
Material / Size #13 #14 #16 #25
Silicone
C-Flex
Viton
ChemDurance Bio
a
Chemdurance Bio tubing is suitable for use with the Smart Sipper for Evolution spectrophotometers
a
Connecting the Sipper Tubing
1. Connect screw connectors to flow cell.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
2. Attach the gooseneck tube.
3. Lower the cell holder into the sample compartment so that the V engages with the groove on the side of the sample compartment and the hold-down magnet engages.
4. Position sipper pump and connect cables.
Note The power supply for the pump is identical to the power supply for the spectrophotometer. There is no risk or danger to connecting “the wrong one”.
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Pump head connection taking silicone tubing to waste
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
5. Decide where the waste container will be placed.
• If very close to the pump, run the pump tubing directly to the waste container.
6. If farther, run (less expensive) PTFE transfer tubing from the pump-head tubing to the waste container.
7. Determine the length of pump tubing required for your configuration. Minimum recommended length of pump tubing is 10 cm.
8. Cut a suitable length of pump head tubing and lay it on the bench in front of the pump.
9. Place the flow cell in the cell holder with the windows in the beam (facing to the front and back).
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1
Zip tie
Turn right to tighten
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
10. Route the PTFE cell connector tubing from the inlet (long connector) through the gooseneck.
Refer to separate Introduction to Sipper Use for detailed information.
11. Route the PTFE cell connector tubing from the outlet (short connector) to the pump.
12. Trim all cell connector tubing to an appropriate length for your use scenario.
13. Attach the pump-head tubing to the PTFE tubing using the couplers.
Secure the connections with zip-ties if using high pump speeds or tubing larger than the size supplied.
14. Install the pump-head tubing into the pump head as shown.
15. Test the system for leaks.
Use the table on the pump to choose a pump speed suitable to the volume that you wish to pump in your procedure.
Note Accuracy of the volume delivered decreases as pumping speed and tubing size increase.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Program a custom sequence to sip at the chosen speed for 60 seconds, or longer if necessary. Place the inlet tube in a beaker of clean solvent and pump for long enough to completely fill the system with solvent and deliver it to the waste container.
Repeat the sip sequence while observing the PTFE tubing between the flow cell and the pump. There should be no bubbles in the tubing. If there are, check the tubing connections to the flow cell.
Remove the flow cell from the cell holder and check it for solvent leaks.
Check the connections between the PTFE tubing and the pump-head tubing for solvent leaks.
16. Follow the process to calibrate the sipper.
Failure to deliver a consistent volume can be an indicator of an air leak at the connection between the cell outlet tubing and the pump-head tubing.
Controlling the Sipper from Software
Two sipper control modes:
1. Uncalibrated – Define pump time at all stages.
2. Calibrated – Define pump volume at each pumping stage.
Sipper parameters are stored in the experimental method. Sipper control is supported only in Quant, Fixed and Scan modes.
See “Sipper Configuration” on page 63 for instructions on programming the sipper.
Sipper setup controls
Selection Definition
Sip Pump in the forward direction
(from the inlet tube towards the flow cell and pump)
Settle Time to wait for the liquid to stop
moving before making a measurement
Air gap Pump air in the forward direction
to push liquid through the system
Rinse Pump rinse solution in the forward
direction
Return Pump in the reverse direction (from
the pump and flow cell towards the inlet tube)
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Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Selection Definition
Measure Record the absorbance
Prompt Display an on-screen prompt to tell
the user what to place at inlet tube for the next step in the sequence
Uncalibrated vs. calibrated sipper operation
Customers whose existing SOPs are based on a prior sipper system that did not support calibration for volume pumped can continue to use time-based pumping in uncalibrated methods.
In general, calibrating the system for volume delivered is the preferred method. Once calibrated, the system will pump the specified volume at each step.

Fiber Optic Coupler and Probe (UV Vis systems only)

1
GENESYS Spectrophotometers
NOTICE Fiber optic cables can suffer damage when bent with too small a radius. A small
radius can also lead to light loss and reduction of performance even if it does not lead to physical damage. The recommended minimum bend radius when working is 20cm.
Note The fiber optic probes that we supply are equipped with a shorter than normal collar at the SMA connector. This helps to maximize the bend radius of the input fiber. Probes purchased from other vendors will generally have a 25 mm long collar at the SMA connector. This will make them difficult to install and may result in an unacceptably small bend radius to the fiber as it exits the collar. If you wish to use a third-party probe, we recommend that you specify a 13 mm collar.
Assembly
Assemble the fibers to the coupler as shown in the photograph.
1. Loosen the three thumb screws on the top cover and remove it from the coupler.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
2. Remove the protective plastic covers from the ends of the fibers.
Save these covers and re-attach them if you remove the probe.
3. Slide the tips of the SMA connector into the receivers and tighten the nuts hand tight.
Do not use tools to tighten the nuts further.
4. Loosen the hold-down thumb-screw, place the fibers under it, and tighten it down to hold the fibers in place.
Do not over-tighten. Be sure to route the cables as shown in the photograph above. This routing pattern maximizes the bend radius.
Note The routing distance for the input and output fibers is slightly different so there will be a small excess loop between the junction nut and the coupler. This is normal and correct.
5. Re-attach the top cover to the coupler.
6. Remove the black rubber cover from the pick-up lens. Be careful not to touch the lens with your fingers.
7. Lower the coupler into the sample compartment with the white arrows aligned.
8. Ensure that the probe tip is tight. It screws on and off in the expected way.
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Configuration 1
GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
Operation
The recommended operation wavelength range is from 220 nm to 1100 nm. Although the fibers are solarization resistant they can suffer cumulative damage (they become opaque) when used at very short wavelengths. Damage to the fibers due to solarization is not covered under warranty.
Two configurations are recommended:
1. Place the probe in a clamp and bring the container with the solution up to it.
2. Hold the probe in your hand and place it into the container with the solution.
Measure the blank solution first and then measure the sample(s) – exactly as you would if you were making measurements with cuvettes.
It is VERY important to avoid having an air bubble in the tip when making a measurement. Air bubbles will result in completely incorrect measurement values. Tap the probe with your finger to knock air bubbles out if using configuration 1. “Shake” the probe back and forth quickly and/or tap it with your finger to knock air bubbles loose if using configuration 2. Do not tap the probe on the side of the container. This could damage the tip or the container.
Probe Tips with Different Pathlengths
While tips with other pathlengths can be purchased for the dip probe we do not recommend their use with the GENESYS systems and have not tested other configurations. Longer pathlengths typically lead to greater light-loss in the tip, reducing photometric range. Shorter pathlengths are more prone to trapping air bubbles in the tip and it is more difficult to shake them loose.
Performance
Fiber optic couplers and probes “cost” light in a spectrophotometer system. Having less light intensity in the system means not being able to deliver the same photometric performance with the fiber probe system that the instrument can deliver with cuvettes in a dark sample compartment. Do not perform the performance verification tests when using the fiber optic probe system.
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GENESYS Spectrophotometers
Spectrophotometer Basics - GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160
As a guide, in our tests, we found the system to very resistant to room lighting conditions and to deliver good linearity to approx. 1.8A and an upper limit of measurement of 2.2A. If performing quantitative analysis with this accessory and measuring above 1A we recommend that users choose a quadratic (second order) fit for the curve and work in an operational range below 1.8A.
Troubleshooting
Problem Cause Solution
Readings are unexpectedly high or low with no consistency to the error
All readings are “off” by a uniform amount
Change in photometric performance – depressed ABS readings or maximum ABS reading
Air bubbles in the tip during sample measurement
Inspect the gap in the tip prior to making a measurement. Take steps to remove any bubbles.
Inconsistent small bend radius Use a large bend radius and keep it
consistent
Air bubble in the tip during blank measurement
Inspect the gap in the tip prior to making the blank measurement. Take steps to remove any bubbles.
Bend radius too small Configure your experimental setup to
use a large and consistent bend radius
Damaged optical fiber Follow the recommendations above.
Record a blank and scan from 1100 nm to 220 nm with deionized water. Save the spectrum. The spectrum should be essentially flat with < ±0.05A baseline noise. Large spikes or discontinuities are common signs of fiber damage.
Try using a different probe if you have one available.
Contact Us
Probe does not work at all – no signal Cover over pick-up lens on coupler Remove the lens cover.
Broken fiber Replace the probe.
Tip loose, damaged or missing Remove and inspect the tip. Ensure
that the mirror is present and clean. Attach the tip and re-test the system.
Coupler not inserted correctly Remove and re-insert the coupler
SMA connector not properly secured
Remove and re-attach the SMA connectors inside the fiber coupler. Ensure that the nuts are not cross threaded.
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Spectrophotometer Basics – All Models

On/Off Accessory
connector
USB-A ports
Network/Ethernet port

Electrical Connections

• Power toggle switch
• 12V DC—connect the cable from the power supply here
• Accessory connector—connect the data cable from the Peltier Thermostatted Cell Holder or Sipper Pump (optional accessories) here
• USB-A ports—see Optional Accessories below
1
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models

Optional Accessories

• Network/Ethernet port—connect a standard Ethernet (RJ45-RJ45) cable between this port and a network port to communicate with the building network
A single USB-A port is located on the front (GENESYS 40 or GENESYS 50) or the side (GENESYS 140, GENESYS 150, GENESYS 180 and BioMate 160) and a pair of USB-A ports is located on the main connector panel (pictured).
The USB ports support the following peripheral devices:
• Special cable to PC to run the instrument from VISIONlite software
• Standard keyboard
• Mouse or touchpad
• Dongle for wireless keyboard/mouse
•Printer
• USB flash memory device
• Barcode reader
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1
Finger hold
Printer housing
Lift
1 2
3
4
5
6
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models

Printer

1. Remove the printer housing cover.
2. Load paper into the optional printer.
Use the finger hold, pull towards you and lift.
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3. Insert printer into GENESYS spectrophotometer.
Guide rails
Guide rails
Connector
Connector
Bottom of printer
Release lever
Back of GENESYS
Serial Number
1
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models
a. Align the guide rail on the printer with the guide rail on the GENESYS
spectrophotometer.
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1
Slide forward Printer fully engaged
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models
b. Push the printer forward until the connectors are fully connected.
You will hear a snap when the connectors have engaged properly.
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Halogen Lamp

Lamp housing connector
Lamp housing guide rail
Lamp
connector
Lamp guide rail
1 2
3
4
Bottom of lamp
Back right corner
The lamp source lifetime is approximately 1,000 hours.
To replace the halogen lamp
1
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models
Thermo Scientific GENEYS Family Spectrophotometers 29
GENESYS 40 shown. GENESYS 140 is similar.
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1
1
2
3
4
5
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models
WiFi Transmitter
1. Print to a wireless printer in the room.
2. Connect to a WiFi router.
NOTICE Prevent damage to the instrument. Remove the WiFi Transmitter from the instrument and package it separately when shipping the instrument – for example to our depot for service.
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Lid Removal and Replacement

Loosen single Phillips/Cross screw as shown and lift lid assembly upwards. Attach new lid in same way.
Lid removal may be required or desired when:
• Installing the Accessory Kit for Hose Entry/Exit on GENESYS 40 or GENESYS 50
1
GENESYS Spectrophotometers
Spectrophotometer Basics – All Models
• Using the Peltier Thermostatted Cell Holder accessory for the 100 series models
• Using the sipper accessory for the 100 series models
• Using the fiber optic probe accessory for the 100 series models
• Using the 8-cell changer for the 100 series models
• Replacing a damaged lid
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GENESYS On-board Software

Settings menu
to view experiment data
to view applications

GENESYS On-board Software Home Screen and Navigation

See Performance Verification Tests
and Reports
When an application is selected, the user is directed to an “Application Home” screen.
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GENESYS On-board Software

Getting Started

Getting Started
On this screen, when available, existing methods can be loaded, new methods created or existing methods modified or edited.
This section provides an overview of the basic operations within an application.
For detailed explanation of parameters within each application and advanced functionality, please see the appropriate section in this manual.
Typically, the Thermo Scientific™ GENESYS™ On-board applications have the following structure and workflows:
•Application Home
View and select methods
Export/Import/Data methods
Select for Smart mode
•Setup
Setup parameters
Configure accessories
Perform calibration for Quant
• Experiment Execution
Perform Blank, begin measurement
Edit sample names
Select sample-specific actions, where applicable
• Data Analysis and Actions
View and analyze data
–Export/print
Save/discard
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Viewing Saved Experiment Data

Data Viewer
Select experiment data by name
2
GENESYS On-board Software
Viewing Saved Experiment Data
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Select method to view details
‘3-dot’ menu presents more method options
Review and use method
Import from network or USB
Sort by name
Select a method as a Smart Method. See SmartStart
Edit to modify the selected method
Create a copy of the selected method and modify parameters
See Importing Methods
GENESYS On-board Software
Viewing Saved Experiment Data

Application Home

This section uses the Scan application as an example. See the specific application section for detailed explanation of parameters and options.
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Long tap to select multiple methods
Delete
Create new method
Edit method name
GENESYS On-board Software
Viewing Saved Experiment Data

Creating A New Method

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All blue text and buttons are editable
See
Accessory Setup
Blue save icon indicates unsaved changes.
Go to previous page
to save
All parameter options are presented in a slide up menu
Follow prompts
to begin experiment
GENESYS On-board Software
Viewing Saved Experiment Data

Experiment Execution

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Swipe right to view method parameters
All measurements are displayed
Print or export
Rename experiment before saving (or use default name)
All experiment data must be saved.
GENESYS On-board Software
Viewing Saved Experiment Data
Example of a printed report. See Printer Setup and Wi-Fi
Printing for details.
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Swipe cursors to points of interest
View values
3-dot for advanced analysis
Scan samples have peak pick options
Tap to edit sample name
Tap sample to highlight in spectrum
Long tap to select multiple
for fine cursor adjustment
to show/hide cursor
GENESYS On-board Software
Viewing Saved Experiment Data

Data Analysis and Actions

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Select Peak Pick
Peaks, Valleys or both
Adjust ABS scale to specify lower limit
Adjust Lambda cursors to specify peak detect range
GENESYS On-board Software
Viewing Saved Experiment Data
Thermo Scientific GENEYS Family Spectrophotometers 41
See Scan Application for detailed information on options and parameters.
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The instrument must be blanked first
GENESYS On-board Software

Live Display Application

Live Display Application
In the live display mode, the instrument performs continuous absorbance measurements automatically.
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Fixed Application

Measure absorbance
Measure transmittance
Select equation template
2
GENESYS On-board Software
Fixed Application
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Selected units will be displayed on the measurement screen and print out.
At most two wavelengths and two factors are supported
Factor values are substituted in the equation and ABS values at defined wavelengths are substituted after measurement
GENESYS On-board Software
Fixed Application
Follow the prompts to complete measurement. When an equation type with two wavelengths is selected, the instrument will acquire measurements at the two selected wavelengths.
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Scan Application

Scan range:
Between 190 nm and 1100 nm for UV-Vis
Between 325 nm and 1100 nm for Vis instruments
Interval:
Specifies how frequently the instrument will acquire a measurement.
In this illustration, data will be captured every 2nm.
Fast, Medium, Slow scan speeds limit the number of data interval options offered
2
GENESYS On-board Software
Scan Application
Speed Interval Options
Fast 5nm, 2nm
Medium 5nm, 2nm, 1nm
Slow
a
0.1 nm interval option is available only on GENESYS 180 instruments
5nm, 2nm, 1nm, 0.5nm, 0.2nm,
a
0.1 nm
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2
To view more sample data options
to run Peak Pick
Three peaks found in the region above the ABS cursor and between wavelength cursors
Adjust wavelength cursors to narrow regions of interest
Adjust ABS cursor to narrow region of interest
Show peaks, valleys or both
Rename data
All data must be saved for data integrity. If a custom name is not provided, the software assigns a default name.
Find the experiment in the Data Viewer using this name
GENESYS On-board Software
Scan Application

Analyzing First Sample

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Quant Application

Add standards and select curve type
The equation type used to fit the standard measurement data is determined by this equation
Selects units in which the sample measurements are displayed and printed
Select if 1 or 2 replicates are needed
Save method
Once sufficient unique standard concentration values are provided, the calibrate button is enabled.
The number of unique standard concentration values are determined from the equation of the curve type.

Calibrated and Uncalibrated Quant Methods

When method is saved after a standard curve is calibrated, the method is saved as a calibrated method. Since the standard curve is already available, it is possible to proceed directly to the sample measurement screen
2
GENESYS On-board Software
Quant Application
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Equation and r-square calculated
Measure is enabled after all standards are measured
Change curve type to find new fit. R-squared value is re-calculated
after sample measurement is complete
New sample
Add standards and select curve type
GENESYS On-board Software
Quant Application
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Cell Changer Setup in Quant

Cell changer with standards
When configuring the cell changer in Quant, the first cell changer will always be configured with standards. The number of standards can only be configured on the Quant Home page. The first cell in the standards cell changer will always be blank.
2
GENESYS On-board Software
Quant Application
For details on how to setup a cell-changer, see Cell Changer Configuration.
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GENESYS On-board Software

C-Mode

C-Mode
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Kinetics Application

Create new method with settings as shown
1 2
Notice measurements are measured every “interval” time
Operation of the Kinetics Application is best explained by walking through an example.
2
GENESYS On-board Software
Kinetics Application
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clock to add more time
to update experiment run time
The experiment run time is updated and chart scaled
Experiment run time may be extended any number of times before experiment run time expires
Complete popup is visible after every measurement is complete
Extend again
Experiment time and chart are updated again
GENESYS On-board Software
Kinetics Application
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Stops the experiment immediately
Adjust cursors
After data acquisition is complete, the Results page is displayed. The linear rate of reaction is calculated.
Slide the cursors to adjust the region where rate is calculated.
Export
Select USB port with flash drive
GENESYS On-board Software

Importing Methods

Importing Methods
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Select location
New folder on USB
New method file on USB
GENESYS On-board Software

Exporting Data and Methods

Exporting Data and Methods

Performance Verification Tests and Reports

Running Performance Verification Tests

Customized Performance Verification Tests

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GENESYS instruments are preconfigured with default Performance Verification Tests. These tests cannot be deleted or edited.
Running a performance verification test is similar to running any other experiment method. Follow the on-screen instructions.
Some Performance Verification Tests can be customized to meet specific verification requirements of users. To customize a test, it must first be duplicated.
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GENESYS On-board Software
Performance Verification Tests and Reports
Often, standard operating procedures require performance verification of instruments periodically. Test such as Stray Light, Wavelength Accuracy and Photometric Accuracy require specific sets of filters and standards. The default performance verification tests are designed to work with specific standards and filters See Table1. However, these tests can be duplicated and customized to work with standards of choice.
Table 1. Description of each test and if it may be duplicated
Performance Verification Test Description
Wavelength Accuracy Xenon This test verifies the wavelength axis performance of the
spectrophotometer.
Scans and locates known xenon emission peaks and verifies that they are found accurately to within the specification for the instrument.
Drift at 500 nm Measures absorbance at 500 nm at 1 minute intervals
for an hour. Measured at 0A (open beam). Blanks and reports maximum deviation from zero. Compares result to specification for the instrument.
Result should be less than the specification.
Noise 0A at 500nm
Records 60 ABS measurements at 1 second intervals. Returns RMS (root mean square) of data set as noise
Noise 1.0A at 500 nm
Noise 2.0A at 500 nm
value and compares specification for the instrument.
Insert 1A or 2A nominal absorbance neutral density glass filter for those measurements.
Result should be less than the specification.
Can Duplicate?
No
No
No
Note: Noise in the GENESYS instruments is so low that the result is reported with more than the usual 3 decimal digits.
Baseline Flatness 1000 to 200 nm Measures any systematic deviation from perfect zero
No when scanning across the common wavelength range. Data is smoothed to remove the impact of noise (noise can be measured separately). Result is the maximum deviation from zero and is compared to the specification for the instrument.
Result should be less than the specification.
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Performance Verification Tests and Reports
Performance Verification Test Description
Stray Light SRE 220 filter (UV-Vis models)
Stray Light SRE 400 Filter (Vis models)
Measures stray light at the specified wavelength.
The filter is a long pass filter that cuts on slightly above the test wavelength. At the test wavelength it should be entirely dark – i.e. 0%T. Longer wavelengths pass through the filter, therefore any transmittance measured at 220 nm is actually photons of longer wavelength that are “stray light”. Sources of stray light include second order effects imperfections in the grating, and imperfections or dirt on mirrors.
The measured transmittance is compared to the specification for the instrument.
Test measures transmittance at the specified wavelength.
Result should be less than the specification.
Can
Duplicate?
Yes
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Performance Verification Tests and Reports
Performance Verification Test Description
Wavelength Accuracy This test verifies the wavelength axis performance of the
spectrophotometer.
Use this test with a calibrated wavelength filter such as the
filter from the SPECTRONIC Standards 2 Kit or
a holmium or didymium glass filter.
User enters the peak wavelengths and calibration uncertainty from the calibration certificate.
The instrument scans across the relevant wavelength range and locates the center of the peak.
Reported wavelength should agree with certificate wavelength to within the sum of the instrument specification and the calibration uncertainty.
Photometric Accuracy This test verifies the photometric (absorbance)
performance of the spectrophotometer.
Use this test with one or more calibrated absorbance filter(s) such as those found in the SPECTRONIC Standards 2 Kit to test accuracy in the visible region. Use calibrated potassium dichromate solution cells, metal on quartz filters, or other recognized calibrated standard
a
materials for the UV region.
Multiple filters calibrated at the same wavelengths but different absorbance values can be configured in a single test.
Can Duplicate?
Yes
Yes
User enters
•calibration wavelengths
• certificate absorbance values
• calibration uncertainty value
from the calibration certificate. User also enters the performance specification for the absorbance value being tested from the specification sheet for the instrument.
b
The instrument measures and reports the absorbance at each specified wavelength. A 1s integration time is used.
Reported absorbance should agree with certificate absorbance to within the sum of the instrument specification for that absorbance level and the calibration uncertainty.
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GENESYS On-board Software
Performance Verification Tests and Reports
a
We recommend against use of didymium glass “dual standard” filters calibrated for both wavelength peaks and photometric accuracy. Customers have reported difficulty in reproducing calibration values for this type of standard although their instruments do reproduce the calibration values for other, more widely accepted and recognized standards. Customers who call for support because an instrument fails a photometric accuracy test with a didymium photometric standard may be required to verify photometric accuracy with a different standard before return shipment for warranty service is authorized.
b
Future releases of software may include a look-up table that populates the instrument specification based on the user-entered certificate absorbance value.

Customizing Stray Light Test

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Save
Set up wavelength
Select target tolerance
Rename
Custom Stray Light performance verification test is created
GENESYS On-board Software
Performance Verification Tests and Reports
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Toggle to perform wavelength repeatability test
GENESYS On-board Software
Performance Verification Tests and Reports

Customizing Wavelength Accuracy Test

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Customizing Photometric Accuracy Test

A typical standards kit for photometric accuracy comes with a Certificate of Calibration. This section illustrates how to configure a photometric accuracy test for custom standard kits.
2
GENESYS On-board Software
Performance Verification Tests and Reports
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Standard ID may be used to identify the corresponding filter in a filter set
Standard ID may be used to identify the corresponding filter in a filter set
GENESYS On-board Software

Accessory Setup

Accessory Setup

Cell Changer Configuration

Cell changer setup in the Scan Application is used as an example in this section. However, the same steps can be followed for all other applications.
Cell changer setup in Quant requires a few extra steps. See Cell Changer Configuration.
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Sipper Configuration

Fast, Medium, Slow Set up the speed of the sipper for an uncalibrated sipper.
These parameter set the time for which the sipper performs this step.
The parameters are applied only when the corresponding step is used in a workflow.
See “Custom Workflows” on page 68
2
GENESYS On-board Software
Accessory Setup
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After configuration,
Configured workflow is Sip, Measure and Rinse
Always blank first
Sipper prompts to allow setting up the blank
when ready
GENESYS On-board Software
Accessory Setup

Measurements

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After sipping, a measurement is made and the rinse stage begins.
GENESYS On-board Software
Accessory Setup
Message provides information and next steps of current state
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Select a speed,
Enter a target value
After sipper completes sipping, measure the sipped volume and enter here.
GENESYS On-board Software
Accessory Setup

Calibrated Sipper

By default, the sipper is configured in an uncalibrated mode. Calibrating a sipper allows precise control over the volume of the liquid drawn.
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New estimated sipping time is calculated from the actual sipped volume
The sipper may be re-calibrated multiple times
Enter new measured volume
1
after calibration is satisfactory
Estimated time is re-calculated
Volume values may be used for setting stage parameters
Parameters can now be set in volume
A rate is calculated
GENESYS On-board Software
Accessory Setup
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1
2
to add new stage
after calibration is satisfactory
GENESYS On-board Software
Accessory Setup

Calibrating the Sipper

The sipper calibration aims to pump 10 mL or a different volume that you specify. We recommend 10 mL as a good choice for most applications. You will require a method to determine how much volume has been pumped. We suggest one of two:
• Pump out of a filled 25 mL graduated cylinder. Note the volume on the scale before and
• Pump out of a weighed beaker or flask. Weigh the beaker again after pumping and

Custom Workflows

If an SOP calls for a specific workflow, the sipper configuration offers customization of workflow.
after pumping. Calculate the volume pumped by subtraction.
calculate the volume pumped by multiplying the difference in mass by the density of the solvent. The density of water can be taken as 1.00 g/mL for most purposes. However, if you require particularly high precision in pumping small volumes you may wish to use purified water and the literature value for density of water at the temperature used.
The workflow will now be saved with the method and will execute with the method.
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Note If the instrument does not detect a sipper, a warning will be displayed. This warning
after setting parameters
Explanation of parameters is provided
Equilibration time in minutes:
anytime to review configuration
parameters
Peltier is setup
will disappear once a sipper is connected.

Peltier Configuration

2
GENESYS On-board Software
Accessory Setup
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anytime Peltier status
If configured, Equilibration countdown begins
GENESYS On-board Software
Accessory Setup
Temperature setpoint:
The instrument starts measurement when the block temperature of the Peltier reaches the temperature setpoint.
Equilibration time in minutes:
Heat transfer from the block to the sample is not instantaneous; the equilibration time acts as delay between when the block temperature reaches the setpoint and when the instrument begins measurement.
Temperature tolerance:
The instrument begins measurement as soon as the Peltier block temperature falls within the temperature tolerance range about the temperature setpoint.
Stir speed:
This parameter ranges from off to 10 and sets the speed at which the stirrer rotates.
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Accessory Configuration in Scan

to set up
Choose accessory type
(in this case, the 8-cell changer)
Prepare cell changer
Match cell configuration to cell changer configuration
Leave blank Skip
Cells 2 through 7 samples
2
GENESYS On-board Software
Accessory Setup
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2
1
2
3
GENESYS On-board Software
Accessory Setup
Remember, first cell always blank Remember, first cell always blank Perform scan analysis on any sample
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2
Equals number of cell changers
Always blank
This blank applied to all subsequent measurements
Others may be configured without restrictions
New blanks applied to subsequent measurements
after replacing cell changer
Next cell changer will start #2 appended
GENESYS On-board Software
Accessory Setup
Measurement will stop after first cell changer.
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to view accessory configuration
GENESYS On-board Software
Accessory Setup
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SmartStart

Mark method as Smart Method
Toggle to unselect.
1
Go to Settings
2
SmartStart™ allows creation of shortcuts to favorite methods on the Home screen.
The Home screen will only show favorite methods.

Configuring and Switching to SmartStart Mode

2
GENESYS On-board Software
SmartStart
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2
3
Instrument in Smart mode
Only Smart Methods displayed
1
Go to Settings
2
3
Normal Mode
GENESYS On-board Software
SmartStart

Exiting SmartStart Mode

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Connecting to VISIONlite

when ready
1 2
3
VISIONlite™ is a PC based software developed by Ascanis and provides the ability to control the GENESYS instruments via a USB cable. VISIONlite needs to be purchased separately and a quote may be provided <need furl from Manas/Kathy Callaghan>. More information on the capabilities of the software may be obtained at <need furl from Manas/Kathy Callaghan>.
After installing VISIONlite, connect the special cable provided with the VISIONlite for GENESYS package between a USB port on the instrument and one on the PC.

Enable the VISIONlite Mode

2
GENESYS On-board Software
Connecting to VISIONlite
When in this mode, the PC will display a notification indicating a GENESYS instrument has been detected. VISIONlite has now connected to the instrument and can be used to capture data and perform advanced calculations.
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GENESYS On-board Software
Connecting to VISIONlite
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Printer Setup and Wi-Fi Printing

1
2
3

Setting Up USB Printer

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5
4
Select USB printer indicated by the USB symbol
Printer Setup and Wi-Fi Printing
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Settings > Network
Select the printer “SSID”
Connect to printer SSID or SSID of the network to which the printer is connected.
Set up the printer
Select printer
Select printer model
Printer Setup and Wi-Fi Printing
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Connect
Preview and print
Preview and print
Printer Setup and Wi-Fi Printing
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Setting Up Thermal Printer

1
2
Confirm the Thermal Printer is installed on the instrument. See Printer for installation instructions.
3
Printer Setup and Wi-Fi Printing
The print option in all applications will only print to the printer configured under settings. repeat the steps and re-configure the printer.
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to access instrument settings

Configuring Network Paths

Configuring Network Paths
When connected to a Wi-Fi or a wired network connection, the instrument can export methods and measurement data to a network location. Multiple network paths may be configured through the Network settings page.

Settings

Setting Description
Smart Start See “SmartStart” on page 25
Languages Selecting a language will set up the locale settings including
Date-Time format and number format. V1.0 of the software does not support multiple languages for the applications.
Display Adjust brightness and toggle screen saver.“Setting Up USB Printer”
on page 79
Sounds Mute or adjust sound volume.
Network Set up the network path.
Printer Set up printing. See “Printer Setup and Wi-Fi Printing” on page 12
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Settings
Setting Description
Date and Time
Disk Space Displays the remaining available instrument memory.
Lamp Status Provides the remaining lamp life in percent.
Software Update
Log Export instrument logs to a USB or a network location. Provide these
logs when asked during service or support.
About This screen provides information about the instrument. Provide this
information when requested during service or support.
VISIONlite Enable connection to VISIONlite from this page.
3
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Settings
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BioMate 160 Applications

Wavelength fixed at 600 nm
Only Peltier accessory allowed
All applications described here are only available on the BioMate 160 instrument.

OD600

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Baseline Correction allows
BioMate 160 Applications

dsDNA

The reference wavelength setting allows the user to correct for any baseline shift caused by scatter from particulates suspended in the sample. This is a relatively common phenomenon in samples that are derived from lyophilized tissue samples. Choose a reference wavelength close to the measurement wavelength(s) where the absorbance of the sample is expected to be zero. The instrument will record the actual absorbance at this wavelength and subtract that value from the “raw” absorbance at the measurement wavelength(s) before performing calculations with that/those data. 340 nm is a commonly accepted reference wavelength for DNA measurements.
Example calculation using a reference wavelength: 260/280 ratio
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RNA
4
BioMate 160 Applications

Protein BCA

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BioMate 160 Applications

Protein Bradford

Protein Bradford method is performed at a wavelength of 595 nm. The workflow is similar to Quant application
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Protein Lowry

4
BioMate 160 Applications
Protein Lowry method is performed at a wavelength of 650 nm. The workflow is similar to Quant application
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BioMate 160 Applications

Protein Pierce 660

Protein Pierce 660 method is performed at a wavelength of 660 nm. The workflow is similar to Quant application
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Protein Rapid Gold BCA

Add a new network path
Protein Rapid Gold BCA method is performed at a wavelength of 660 nm. The workflow is similar to Quant application.
4
BioMate 160 Applications
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Custom name to identify path
Full network path in the format shown Toggle if the path requires authentication
If network location requires authentication, follow the prompts
Save location after all fields are filled
BioMate 160 Applications
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