Biotek MultiFlo FX Operator's Manual

Operator’s Manual
Microplate Dispenser
MultiFlo™ FX Microplate
Dispenser
MultiFlo™ FX Multi-Mode Dispenser Operator's Manual
BioTek Instruments, Inc. May 2014 © May 2014 Part Number 1261000 Revision B
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Notices

BioTekInstruments, Inc.
Highland Park, P.O. Box 998
Winooski, Vermont 05404-0998 USA

All Rights Reserved

© 2014, BioTek®Instruments, Incorporated. No part of this publication may be reproduced, transcribed, or transmitted in any form, or by any means electronic or mechanical, including photocopying and recording, for any purpose other than the purchaser’s use without written permission of BioTek Instruments, Inc.

Trademarks

BioTek®is a registered trademark and MultiFlo™ FX Multi-Mode Dispenseris a trademark of BioTek Instruments, Inc.
Microsoft®, Internet Explorer®, Windows®, Windows 7, Windows 8, Windows Vista®, Windows XP, and Excel®are either registered trademarks or trademarks of Microsoft Corporation in the United States and/or other countries.
All other trademarks are the property of their respective holders.

Restrictions and Liabilities

Information in this document is subject to change and does not represent a commitment by BioTek Instruments, Inc. Changes made to the information in this document will be incorporated in new editions of the publication. No responsibility is assumed by BioTek for the use or reliability of software or equipment that is not supplied by BioTek or its affiliated dealers.
MultiFlo™ FX Multi-Mode Dispenser
Notices|iii
Contents
Notices ii
All Rights Reserved ii Trademarks ii Restrictions and Liabilities ii
Global Service and Support ix Revision History x Document Conventions xi Intended Use Statement xi Quality Control xi Warranty and Product Registration xii Dispense Cassette Warranty xii Repackaging and Shipping xii Warnings xii Hazards and Precautions xiii
Hazards xiii Precautions xiv
CE Mark xvi
Directive 2004/108/EC: Electromagnetic Compatibility xvi Directive 2006/95/EC Low Voltage (Safety) xvi Directive 2002/96/EC: Waste Electrical and Electronic Equipment xvii Directive 98/79/EC: In Vitro Diagnostics (if labeled for this use) xvii
Electromagnetic Interference and Susceptibility xvii
USA FCC CLASS A xvii Canadian Department of Communications Class A xviii
User Safety xviii Safety Symbols xix
Introduction 1
Introducing the MultiFlo™ FX Dispenser 2 Features of the MultiFlo FX 3
Washer 3 Peri-pump Dispenser 4 Syringe Dispensers 4 Liquid Handling Control™ (LHC) Software 5 RAD™ Technology Features 5 MultiFlo FXModels 6
MultiFlo FX Dispenser Comparison 7
Plate Types Table 9
BioStack Compatibility 10 Package Contents 12 Optional Accessories 13
Peri-pump Optional Accessories 13 Syringe Dispenser Optional Accessories 14
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Strip Washer Optional Accessories 15
Physical Specifications 18 Performance Specifications 21
Peri-Pump Dispenser 21 Syringe Dispensers 22 Strip Washer 23
Space Requirements 25 BioTek's Customer Resource Center 26
Installation 27
Unpack and Inspect the Instrument 28 Install the Waste Tubing 29 Remove the Shipping Hardware 31 Set up the Strip Washer 34
Strip Washer accessories 34 Attach washer module and connect its cable 35 Install the tubing bracket 37 Install the Fluid Supply 38 Install the Waste Bottle 39 Install the muffler 41 Install Washer Manifolds 41
Set Up the Peri-pump Dispenser 44
Attach the Peri-pump Cover Panel 44
Install the Secondary Peri-Pump 46 Install RAD Technology Components 51
Install the Tubing Bracket and RADModule 51 Install the tubing bracket 52 Attach the RADModule to the Tubing Bracket 52 Install RAD Dispense Head 53 Dispense Cassette Diagram 54 Install the Dispense Cassette 56 Install RAD Technology Cassette 58 Prime Trough Inserts 59 Peri-pump Reservoir Holder 60 Shorten the Dispense Cassette Tubing 61
Install the Syringe Dispenser Component 62
Syringe Dispenser Placement Options 63 Install the Syringe Dispenser on Back Shelf 64 Install the Syringe Dispenser on Top 65 Install Tubing and Manifolds for Syringe Dispenser 68 Syringe Dispenser Check Valves 70 Install Inline Filter for 32-Tube Dispensers 71
Install Software/Connect to Computer 71
Connect to Host Computer 72
Connect Power Cable 72 Define Instrument Settings 73
LHC Users Only 73 Enable Waste Sensor 73
MultiFlo™ FX Multi-Mode Dispenser
Notices|v
Update the Instrument to use the Syringe Dispenser 74 Change the Syringe Dispenser Manifold 75 Change the cassette type setting 76 Setting the Time and Date 77 Define Startup Preferences (LHC users only) 77
Verify Performance 79
Verify the Peri-Pump Dispenser 80 Verify the Syringe Dispensers 80 Verify the Washer Component 81
Repacking the MultiFlo FX 82 Install the Shipping Hardware 83 Repacking the Secondary Peri-pump 85 MultiFlo FX Repacking 86 Repacking the Syringe Dispenser 89 Repacking the Strip Washer 90
Operation 91
Touch Screen Basics 92
Quick Prime 93 Quick Dispense 94 Quick Wash 95 Add protocols to the Home screen 95 Remove protocols from the Home screen 95 Get protocols from a memory stick - USB drive 96 Hardware Change Detected 96
Optimize Performance 98
Recommended prime volumes for the Strip Washer 99 Recommended prime volumes for the Peri-pump 99 Recommended prime volumes for the Syringe dispensers 101 Optimize protocols to improve evacuation 101 Add a secondary aspiration to a wash cycle 101
Create or Modify a Protocol 102 Protocol Parameters Tables 103 Wash Parameters Table 108
Washer Flow Rates 111 Pre-Dispense 113 Minimum Prime Volumes for the Strip Washer 114 Bottom Wash 114 Change the Plate Type 115 Rename a protocol 115 Shake/Soak Step Parameters 116 Repeat steps in a Loop 116 Delay the Protocol 117 Timer Activated Delay 118 RUN: Running Predefined Protocols 120 LHC Users Only: Customize the Predefined Protocols 120
Predefined Protocols Listing 121 Predefined Sample Protocols 122 Operating with the BioStack 124
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Use the BioStack 125 Re-stack plates in the BioStack 127 Nth Plate to perform special process 127 About the Nth Plate Step 128
Advanced Plate Sequencing with the BioStack 129 Plate Types and Processing Patterns 133 Handling Special Plates and Mini-tubes 134
1536F - 1536-well Flanged Plates 134 Peri-pump Special Plate Handling 134 Special Plate Carrier for Mini-tubes 136 Mini-Tube Racks 137 Dispensing to Mini-Tubes 137
Dispense Processing Patterns 138
8-Channel Dispenser Dispense Pattern 139 Dispense Pattern with Both Syringes 140
Washer Operation 141
About the MultiFlo FX Wash Step 141
Cell Wash 142
Define a Cell Wash Protocol 142 Cell Wash Strategies 143
Biomagnetic Separation - Magnetic Bead Assays 145
Perform Magnetic Bead Assays 146 Optimize Magnetic Bead Protocols 147 Flat Magnets 147 Ring Magnets 148 How to determine the Magnet Adapter Height Offset 149 Magnet Height Offset 150 Special Procedure for Magnetic Bead Assays 151
Peri-pump Peristaltic Dispenser 152 Peri-pump: How it works 153
Release the tension on the dispense cassette 154
Peri-pump Dispense Step 155
RADTip Tracking 156 RAD Well Map 157
Require a Specific Peri-pump Cassette 158 Peri-pump Advanced Settings 159
Settings for 0.5 µL Dispense 159 8-to-1 Tube RAD Cassette 159
Dual Syringe Dispenser 160
How to Prime the Syringe dispenser 160
Syringe Prime Step 161 Syringe Dispense Step 163
Change the Syringe Dispenser Manifold 165
Syringe Dispenser Settings 166 Syringe Dispenser- Autoclavable vs. Non-autoclavable 167 Changing the Instrument's Settings 168
Dispense Pattern 168
MultiFlo™ FX Multi-Mode Dispenser
Notices|vii
Change the Plate Carrier Setting (Touch screen) 169 Change the Plate Clearance Setting (Touch screen) 169 Plate Carrier Speed 170 Upload-Download Protocols (LHC Only) 170 Transfer Protocols (Touch Screen Only) 170 Transfer Plate Lid Definitions 171
Maintenance 173
Overview 174 Recommended Maintenance Schedule 176 Daily Maintenance 178 Overnight/Multi-Day Maintenance 179 AutoPrime 179
Turn on AutoPrime for the Peri-pump Dispenser 180 Turn on AutoPrime for the Syringe Dispenser 182 Turn on AutoPrime for the Washer 183
Soak the manifold tubes in cleaning fluid 185 Removing Protein Residuals and Fungi Growth 187 Periodic Maintenance 189
Autoclavable Components 190 Clean the Bottles 190 Clean the Plate Carrier 191 Clean the exterior surfaces 191
Peri-pump Dispenser Maintenance 192
Flush the Dispense Cassette 192 Unclog the Dispense Tips 194 RADSingle-tube Cassette - Unclog the Tip 196 RAD8-to-1 Cassette - Unclog the Tips 197 Record the Number of Plates Processed 199 RAD8-to-1 Cassette - Replace Chute 200
Syringe Dispenser and Strip Washer Maintenance 201
Clean the Manifolds 201 Clean the Dispense/Aspirate Tubes 202 Clean or Replace the Check Valves 204 Autoclave the Syringe Head 204
Decontamination 205
Tools and Supplies 206 Decontaminate Exterior Surfaces 207 Decontaminate Tubing and Manifold 208
Long Shutdown (Prepare for Storage or Shipment) 208
Storing the Instrument 210
Replace Components 210 Calibrate the Backlash for Syringe Dispenser 212
Qualification 215
Qualification Overview 216
Washer 216 Peri-pump and Syringe Dispensers 216
Qualification Schedule 217
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Index..........................................................................................
System Self-Test, Verify Information 218
Record Onboard Software 218
Liquid Testing the MultiFlo™ FX Multi-Mode Dispenser 219
Which Tests to Perform? 219 Important Recommendations for All Liquid Tests 220
Peri-pump Dispense Precision and Accuracy Tests 221
Peri-pump Dispenser Test Materials 223 Peri-pump Dispenser Precision and Accuracy Test Solutions 223
Perform the Peri-Pump Precision and Accuracy Tests 224 Syringe Dispenser Liquid Tests 235
Syringe Dispenser Test Materials 236 Syringe Dispenser Test Solutions 236
Perform the Syringe Dispense Precision & Accuracy Test 236 Washer Qualification Liquid Tests 250
Dispense Precision and Accuracy Test 250 Evacuation Efficiency Test 250 Washer Qualification Test Materials 251 Create Washer Qualification Protocols 252 Dispense Precision and Accuracy Test 253 Evacuation Efficiency Test 254 Evacuation Diagnostic Test 256
Troubleshooting 271
Troubleshooting 272
Syringe Dispenser Troubleshooting 273 Dispense Manifold Movement 273 Fluid Delivery 274 Fluid Leakage 276 Microplate Carrier Movement 276 Syringe Movement 277 Peri-pump Troubleshooting 277 Washer Troubleshooting 278 Fluid Aspiration 278 Fluid Delivery 280 Fluid Leakage 282
Error Codes 283
System Error Codes 284 MultiFlo FX Software Error Codes 294
Chemical Compatibility 306
301
MultiFlo™ FX Multi-Mode Dispenser
Global Service and Support| ix

Global Service and Support

BioTek instrument service and repair is available worldwide at several of BioTek’s International Service Centers and in the field at your location. Contact the office nearest you to arrange service or to get answers to your technical questions, call the Technical Assistance Center (TAC) at 802-655-4740 in the US.
BioTek World Headquarters US BioTek China
Mailing Address: PO Box 998, Highland Park Winsooki, VT 05404-0998 United States
Service Shipping Address: 15 Tigan Street Winooski, VT 05404 United States
Phone: (800) 242-4685 Fax: (802) 654-0638
Email: TAC@biotek.com Website: www.biotek.com
BioTek Germany Service Center & European Coordination Center
Kocherwaldstrasse 34 D-74177 Bad Friedrichshall Germany
Phone: +49 (0) 71369680 Fax: +49 (0) 7136968111
Room 304, Tower D Ocean International Center 62 Middle 4th East Ring Road Chaoyang District Beijing 100024 P.R. China
Phone: +86 (10) 85865569 Fax: +86 (10) 85861829
Email: infochina@biotek.com Website: www.biotekchina.com.cn
BioTek Instruments SAS
Bureau de liaison France
50 avenue d’Alsace 68025 Colmar Cedex France
Phone: +33 (3) 89206329 Fax: +33 (3) 89204379
Email: info@biotek.de Website: www.biotek.de
Email: info@biotek.fr Website: www.biotek.fr
BioTek India BioTek Singapore
Unit 223, Linkway Estate New Link Road, Malad West Mumbai 400064 India
Phone: +91 (22) 28789966 Fax: +91 (22) 28759944
Email: biotek@biotek.in Email: singapore@biotek.in
20 Science Park Road #01-08A Teletech Park Singapore 117674
Phone: +65 65922100 Fax: +65 67772611
BioTek Instruments, Inc.
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BioTek India BioTek Singapore
Website: www.biotek.in Website: www.biotek.com
BioTek South Korea BioTek Switzerland
3F, Gyungnam building, 830-48 Yeoksam-dong, Gangnam-gu Seoul, South Korea (135-936)
Phone: +82 (0) 2-562-4740 Fax: +82 (0) 2-562-4750
Email: korea@biotek.com Website: www.biotekinstruments.co.kr
Zentrum FanhÖfli 8 6014 Luzern Switzerland
Phone: +41 (41) 2504060 Fax: +41 (41) 2505064
Email: info@biotek.ch Website: www.biotek.ch
BioTek United Kingdom (UK) BioTek Japan
6 Bull Street Potton, Bedfordshire SG19 2NR United Kingdom
Phone: +44 (1767) 262000 Fax: +44 (1767) 262330
Email: info@biotek.uk.com Website: www.biotek.uk.com
8F Andoh Building 2-7-1 Taito, Taito-ku Tokyo 110-0016 Japan
Phone: +81 (0)3 5812 8109 Fax: +81 (0)3 5812 8115
Email: infojapan@biotek.com Website: www.biotek.com/ja

Revision History

Rev Date Changes
A 10/2013 First Issue
B 5/2014 The manual was updated to add RAD Technology content
throughout. Syringe dispenser installation steps were updated to add the "Import from USB" calibration data feature. Added references to new Peri-pump cassette types and new Syringe dispenser manifolds. Added references to and some instructions for running the BioStack 4 to process microplates with lids. Updated the contents of the Cassette Calibration folder to match improvements made to its separately purchased accessory kit: PN7170017. Refined the procedure to remove proteins from the tubing by emphasizing the need to flush first with buffer.
MultiFlo™ FX Multi-Mode Dispenser

Document Conventions

This manual uses the following typographic conventions:
n This note format calls attention to important information.
Warnings are presented in this style to call attention to potential hazards and
other safety concerns.
This icon calls attention to important safety information.
Document Conventions| xi
Tips and suggestions for improving performance are formatted this way.
Navigation instructions: how to get to the function being described

Intended Use Statement

l The MultiFlo™ FX Multi-Mode Dispenser provides microplate priming and dispensing, and
when equipped, washing, for ELISA™, fluorescence and chemiluminescence immunoassays, cellular and agglutination assays.
l If the instrument has an "IVD" label it may be used for clinical and non-clinical purposes,
including research and development. If there is no such label the instrument may only be used for research and development and non-clinical purposes.

Quality Control

It is considered good laboratory practice to run laboratory samples according to instructions and specific recommendations included in the assay package insert for the test to be conducted. Failure to conduct Quality Control checks could result in erroneous test data.
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Warranty and Product Registration

Please take a moment to review the Warranty information that shipped with your product. Please also register your product with BioTek to ensure that you receive important information and updates about the product(s) you have purchased.
You can register online through BioTek’s Customer Resource Center (CRC) at
www.biotek.com or by calling 888/451-5171 or 802/655-4740.

Dispense Cassette Warranty

The Peri-pump dispense cassettes are backed by BioTek's Confidence-Plus lifetime warranty. For the lifetime of the cassette, BioTek guarantees the cassette components (Tip Holder, Center Holder, Tube Tensioner, and Tube Organizer) will withstand steam autoclave conditions of 121°C and 1 bar (750 mmHg) without adversely affecting dispense performance. In the event of a failure of any cassette component previously listed, BioTek will replace the cassette components free of charge.

Repackaging and Shipping

If you need to ship the instrument to BioTek for service or repair, contact BioTek for a Return Materials Authorization (RMA) number and use the original packing materials. Other forms of commercially available packaging are not recommended and can void the warranty. If the original packing materials have been damaged or lost, contact BioTek for replacement packing.

Warnings

Operate the instrument on a level, stable surface away from excessive humidity. When operated in a safe environment, according to the instructions in this document, there are no known hazards associated with the MultiFlo FX. However, the operator should be aware of certain situations that could result in serious injury; these vary depending on the instrument type. See Hazards and
Precautions.
Strict adherence to instrument maintenance and qualification procedures is required to ensure accurate dispense volumes and risk-free operation.
MultiFlo™ FX Multi-Mode Dispenser

Hazards and Precautions

Hazards

The following hazards are provided to help avoid injury:
Warning! Power Rating. The instrument’s power supply or power cord must be connected to a power receptacle that provides voltage and current within the specified rating for the system. Use of an incompatible power receptacle may produce electrical shock and fire hazards.
Warning! Electrical Grounding. Never use a plug adapter to connect primary power to the external power supply. Use of an adapter disconnects the utility ground, creating a severe shock hazard. Always connect the power cord directly to an appropriate receptacle with a functional ground.
Warning! Service. Only qualified technical personnel should perform service procedures on internal components.
Hazards and Precautions| xiii
Warning! Accessories. Only accessories which meet the manufacturer’s specifications shall be used with the instrument.
Warning! Lubricants. Do not apply lubricants to the microplate carrier or carrier track. Lubricant on the carrier mechanism will attract dust and other particles, which may obstruct the carrier path and cause the instrument to produce an error.
Warning! Liquids. Avoid spilling liquids on the instrument; fluid seepage into internal components creates a potential for shock hazard or instrument damage. If a spill occurs while a program is running, abort the program and turn the instrument off. Wipe up all spills immediately. Do not operate the instrument if internal components have been exposed to fluid.
Warning! Unspecified Use. Failure to operate this equipment according to the guidelines and safeguards specified in this manual could result in a hazardous condition.
Warning! Software Quality Control. The operator must follow the manufacturer’s assay package insert when modifying software parameters and establishing washing or dispensing methods. Failure to conduct quality
control checks could result in erroneous test data. Warning! Internal Voltage. Always turn off the power switch and unplug the
power supply before cleaning the outer surface of the instrument.
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Warning! Potential Biohazards. Some assays or specimens may pose a biohazard. Adequate safety precautions should be taken as outlined in the assay’s package insert. This hazard is noted by the symbol shown here. Always wear safety glasses and appropriate protective equipment, such as chemically resistant rubber gloves and apron.
Warning! Pinch Hazard. Some areas of the instrument or its components can present pinch hazards when the instrument is operating. Depending on the instrument or component, these areas are marked with the symbol shown here. Keep hands/fingers clear of these areas when the instrument is operating.

Precautions

The following precautions are provided to help avoid damage to the instrument:
Caution: Service. The instrument should be serviced by BioTek authorized service personnel. Only qualified technical personnel should perform troubleshooting and service procedures on internal components.
Caution: Spare Parts. Only approved spare parts should be used for maintenance. The use of unapproved spare parts and accessories may result in a loss of warranty and potentially impair instrument performance or cause damage to the instrument.
Caution: Environmental Conditions. Do not expose the instrument to temperature extremes. For proper operation, ambient temperatures should remain within the range listed in the Specifications section. Performance may be adversely affected if temperatures fluctuate above or below this range. Storage temperature limits are broader.
Caution: Sodium Hypochlorite. Do not expose any part of the instrument to the recommended diluted sodium hypochlorite solution (bleach) for more than 20 minutes. Prolonged contact may damage the instrument surfaces. Be certain to rinse and thoroughly wipe all surfaces.
Caution: Buffer Solution. Although many precautions have been taken to ensure that the instrument is as corrosion-proof as possible, the instrument is not sealed and liquids can seep into sensitive components. Make sure that any spilled buffer solution is wiped off the instrument. Prolonged exposure to salt solution may corrode parts of the microplate carrier, movement rail, springs, and other hardware.
Caution: Chemical Compatibility. Some chemicals may cause irreparable damage to the instrument. The following chemicals have been deemed safe for use in the instrument: buffer solutions (such as PBS), saline, surfactants, deionized water, 70% ethyl, isopropyl, or methyl alcohol, 40% formaldehyde, and 20% sodium hydroxide. Never use acetic acid, DMSO, or other organic solvents. These chemicals may cause severe damage to the instrument.
MultiFlo™ FX Multi-Mode Dispenser
Hazards and Precautions| xv
Contact BioTek for more information and prior to using other questionable chemicals.
Caution: Bovine Serum Albumin. Solutions containing proteins, such as bovine serum albumin (BSA), will compromise the instrument’s performance over time unless a strict maintenance protocol is adhered to. See Maintenance procedures regarding BSA.
Caution: Power Supply. Only use the power supply shipped with the instrument. Operate this power supply within the range of line voltages listed on it.
Caution: Disposal. This instrument contains printed circuit boards and wiring with lead solder. Dispose of the instrument according to Directive 2002/96/EC, “on waste electrical and electronic equipment (WEEE),” or local ordinances.
Caution: Warranty. Failure to follow preventive maintenance protocols may void the warranty.
Caution: Shipping Hardware. All shipping hardware (e.g., shipping bracket
etc.) must be removed before operating the instrument and reinstalled before repackaging the instrument for shipment.
Caution: Do not run the Peri-pump without a cassette installed on the pump. Caution: Electromagnetic Environment. Per IEC 61326-2-6 it is the user’s
responsibility to ensure that a compatible electromagnetic environment for this instrument is provided and maintained in order that the device will perform as intended.
Caution: Electromagnetic Compatibility. Do not use this device in close proximity to sources of strong electromagnetic radiation (e.g., unshielded intentional RF sources), because these may interfere with the proper operation.
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CE Mark

Based on the testing described below and information contained herein, this instrument bears the CE mark.
n Note: See the Declaration of Conformity for specific information.

Directive 2004/108/EC: Electromagnetic Compatibility

Emissions—Class A
The system has been type-tested by an independent, accredited testing laboratory and found to meet the requirements of EN 61326-1: Class A for Radiated Emissions and Line Conducted Emissions.
Verification of compliance was conducted to the limits and methods of EN 55011 (CISPR 11) Class A. In a domestic environment it may cause radio interference, in which case, you may need to mitigate the interference.
Immunity
The system has been type-tested by an independent, accredited testing laboratory and found to meet the requirements of EN 61326-1 and EN 61326-2-6 for Immunity. Verification of compliance was conducted to the limits and methods of the following:
EN 61000-4-2, Electrostatic Discharge
EN 61000-4-3, Radiated EM Fields
EN 61000-4-4, Electrical Fast Transient/Burst
EN 61000-4-5, Surge Immunity
EN 61000-4-6, Conducted Disturbances from RFI
EN 61000-4-11, Voltage Dips, Short Interruptions and Variations

Directive 2006/95/EC Low Voltage (Safety)

The system has been type-tested by an independent testing laboratory and was found to meet the requirements of this Directive. Verification of compliance was conducted to the limits and methods of the following:
MultiFlo™ FX Multi-Mode Dispenser
Electromagnetic Interference and Susceptibility| xvii
EN 61010-1, “Safety requirement for electrical equipment for measurement, control and laboratory use. Part 1, General requirements.”
EN 61010-2-081, “Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes.”

Directive 2002/96/EC: Waste Electrical and Electronic Equipment

Disposal Notice: This instrument contains printed circuit boards and wiring with lead solder. Dispose of the instrument according to Directive 2002/96/EC, “on waste electrical and electronic equipment (WEEE)” or local ordinances.

Directive 98/79/EC: In Vitro Diagnostics (if labeled for this use)

l Product registration with competent authorities. l Traceability to the U.S. National Institute of Standards and Technology (NIST).
EN 61010-2-101 Particular requirements for in vitro diagnostic (IVD) medical equipment.

Electromagnetic Interference and Susceptibility

USA FCC CLASS A

RADIO AND TELEVISION INTERFERENCE
NOTE: This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference, in which case the user will be required to correct the interference at their own expense.
In order to maintain compliance with FCC regulations shielded cables must be used with this equipment. Operation with non-approved equipment or unshielded cables is likely to result in interference to radio and television reception.
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Canadian Department of Communications Class A

This digital apparatus does not exceed Class A limits for radio emissions from digital apparatus set out in the Radio Interference Regulations of the Canadian Department of Communications.
Le present appareil numerique n'émet pas de bruits radioelectriques depassant les limites applicables aux appareils numerique de la Class A prescrites dans le Reglement sur le brouillage radioelectrique edicte par le ministere des Communications du Canada.

User Safety

This device has been type-tested by an independent laboratory and found to meet the requirements of the following:
l Underwriters Laboratories UL 61010-1 “Safety requirements for electrical
equipment for measurement, control and laboratory use; Part 1: general requirements.”
l Canadian Standards Association CAN/CSA C22.2 No. 61010-1 “Safety
requirements for electrical equipment for measurement, control and laboratory use; Part 1: general requirements.”
l EN 61010 Standards, see CE Mark on page xvi.
MultiFlo™ FX Multi-Mode Dispenser

Safety Symbols

Some of these symbols appear on the instrument or accessories:
Alternating current Courant alternatif Wechselstrom Corrientealterna Correntealternata
Safety Symbols| xix
Both direct and alternating current Courant continu et courant alternatif Gleich - und Wechselstrom Corriente continua y corrientealterna Corrente continua e correntealternata
Direct current Courant continu Gleichstrom Corriente continua Corrente continua
On (Supply) Marche (alimentation) Ein (VerbindungmitdemNetz) Conectado Chiuso
Off (Supply) Arrêt (alimentation) Aus (TrennungvomNetz) Desconectado Aperto (sconnessionedallaretedialimentazio ne)
Warning, risk of electric shock Attention, risque de choc électrique Gefährlicheelektrischeschlag Precaución, riesgo de sacudidaeléctrica Attenzione, rischiodiscossaelettrica
Earth ground terminal Borne de terre Erde (Betriebserde) Borne de tierra Terra (difunzionamento)
Protective conductor terminal Borne de terre de protection Schutzleiteranschluss Borne de tierra de protección Terra diprotezione
Caution (refer to accompanying documents) Attention (voir documents d’accompanement) AchtungsieheBegleitpapiere Atención (vease los documentosincluidos) Attenzione, consultare la doc annessa
Warning, risk of crushing or pinching Attention, risqued’écrasement et pincement Warnen, Gefahr des Zerquetschens und Klemmen Precaución, riesgo del machacamiento y sejeción Attenzione, rischiodischiacciareedintrappolarsi
Warning, hot surface Attention, surface chaude Warnen, heißeOberfläche Precaución, superficiecaliente Attenzione, superficiecalda
In vitro diagnostic medical device Dispositif médical de diagnostic in vitro Medizinisches In-Vitro-Diagnostikum Dispositivo médico de diagnóstico in
Warning, potential biohazards Attention, risquesbiologiquespotentiels Warnung! MoeglichebiologischeGiftstoffe Atención, riesgosbiológicos Attenzione, rischiobiologico
Separate collection for electrical and electronic equipment Les équipements électriques et électroniques font l’objet d’une collecte sélective
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vitro Dispositivo medico diagnostico in vitro
Consult instructions for use Consulter la notice d’emploi Gebrauchsanweisung beachten Consultar las instrucciones de uso Consultare le istruzioni per uso
Getrennte Sammlung von Elektro­und Elektronikgeräten Recogida selectiva de aparatos eléctricos y electrónicos Raccolta separata delle apparecchiature elettriche ed elettroniche
MultiFlo™ FX Multi-Mode Dispenser
Chapter 1

Introduction

Thank you for purchasing the MultiFlo™ FX Multi-Mode Dispenser. This chapter describes the instrument's features and specifications and includes important contact information.
Introducing the MultiFlo™ FX Dispenser 2 Features of the MultiFlo FX 3 MultiFlo FX Dispenser Comparison 7 BioStack Compatibility 10 Package Contents 12 Optional Accessories 13 Physical Specifications 18 Performance Specifications 21 Space Requirements 25 BioTek's Customer Resource Center 26
2 | Chapter 1: Introduction

Introducing the MultiFlo™ FX Dispenser

The MultiFlo FX offers several devices in one instrument: one or two peristaltic pump dispensers called the Peri-pump, a dual Syringe pump dispenser, and either a strip Washer or a single-channel Random Access Dispenser (RAD) module. The MutliFlo FX is available in multiple configurations to support numerous microplate geometries.
Device/Component Description
1 Peri-pump Dispenser Peristaltic, 8-channel dispenser with entirely visible fluid
path.
2 Dispense arm Holds the Peri-pump Tip Holder(s), the Syringe dispenser
manifolds and the washer dispense manifold, when applicable.
MultiFlo™ FX Multi-Mode Dispenser
Features of the MultiFlo FX | 3
Device/Component Description
3 Aspirate/RAD arm Washer and RAD models only: holds the strip washer's
aspirate manifold or the RAD cassette's tip holder.
4 Priming trough Waste reservoir for collecting or disposing of priming fluid.
Priming trough inserts, for collecting fluid, are shown in this image.
5 Plate Carrier Holds standard microplates for processing.
6 Touch screen One of two ways to control the MultiFlo FX; the other way is
LHC.
7 Strip Washer An external module containing a syringe-pump dispenser
and vacuum aspiration pump.
8 Syringe Dispenser Another external module with two distinct syringe-pump
dispensers that support a variety of manifold types to process standard and low-density microplates.
9 Peri-pump Dispenser Secondary or external Peri-pump dispenser (required for
RAD models).
See Plate Types Table on page 9 to review the plate types supported by each
device.

Features of the MultiFlo FX

l Supports all microplate-based assays, including ELISA, fluorescence,
chemiluminescence, RIA, DNA probes, and cellular assays.
l A variety of solutions, including buffered saline and reagents can be dispensed.
l The intuitive onboard software allows you to create and store wash and dispense
protocols. BioTek provides numerous predefined protocols for maintenance and instrument qualification purposes.
l Two USB flash drive ports facilitate file transfer and storage.
l A low-maintenance design, the result of BioTek’s long history with liquid-handling
instruments.
l Compatible with BioTek’s BioStack™ Microplate Stacker for automated plate processing.
l A robot-accessible carrier that can be interfaced into some robotic systems.
l Computer control using BioTek’s Liquid Handling Control™software (“LHC”).

Washer

BioTek Instruments, Inc.
4 | Chapter 1: Introduction
l Programmable dispense volumes, and a wide range of wash options, from gentle
washing for cellular assays to vigorous washing for ELISA.
l A “bottom washing” routine to lower the background absorbance and “crosswise” or
secondary aspiration to reduce residual volumes.
l Supports Wash, Prime, Dispense, and Aspirate steps.
l Several predefined protocols are provided to simplify preventative maintenance, which
should be performed regularly to ensure optimum washer performance.

Peri-pump Dispenser

l A peristaltic pump with eight individual tubes transfers fluid from a supply bottle, or up
to eight different supply bottles, to various vessels. The pump has four rollers over which the tubing is stretched.
l The tubing is contained in an easy to load and unload cassette that is attached to the
pump head. The pump’s protective cover must be in place to run a dispense routine.
l Three tubing sizes are available: 1 µL, 5 µL, and 10 µL for the most precise dispensing of
volumes from 1 to 30,000 µL and 0.5 µL dispenses when using a 1 µL cassette.
l RAD™ Technology models support "random access dispensing" with several single-
channel cassette options, including a bulk dispensing cassette (8 tubes to one chute) with flow tracking to minimize turbulence in the wells.
l Autoclavable tubing (steam temperatures and pressures of 121° C and 1 bar
(750 mmHg)) is compatible with 70% ethyl or isopropyl alcohol and 0.5% sodium hypochlorite (bleach) solution for easy maintenance.

Syringe Dispensers

l The Syringe dispenser has a long-lasting seal that ensures precise and accurate fluid
delivery, as well as reproducibility for repeated dispenses.
l Two syringe pumps support distinct fluid sources and dispense manifolds:
o
16-channel: one tube per well for 384-well plates and two tubes per well for 96­well plates.
o
32-channel: one tube per well for 1536-well plates.
o
8-channel (two manifolds in one block): one tube per well for both 96- and 384­well plates.
l Autoclavable components can be used with organic solvents and provide easy
maintenance.
l Does not require recalibration
Low-density Microplate-specific Syringe Manifolds
Plate-specific dispense manifolds with angled dispensing for cellular assays:
MultiFlo™ FX Multi-Mode Dispenser
Features of the MultiFlo FX | 5
l 6-well plate: 8-channel dispense manifold (4 tubes/well).
l 12-well plate: 9-channel dispense manifold (3 tubes/well).
l 24-well plate: 8-channel dispense manifold (2 tubes/well).
l 48-well plate: 12-channel dispense manifold (2 tubes/well).

Liquid Handling Control™ (LHC) Software

BioTek’s Liquid Handling Control (LHC) software lets you control the instrument from your computer. You’ll enjoy the convenience of programming assay-specific wash and dispense protocols in a familiar Windows environment (Microsoft Windows®7, Windows 8, and Windows XP).
For high-throughput applications, the LHC supports BioStack™ integration.
Please refer to the LHC Installation Guide and Help system to learn about:
o
Installing the LHC software on the controlling computer
o
Running Maintenance protocols
®
o
Running Qualification protocols
o
Special considerations when operating with the BioStack Microplate Stacker

RAD™ Technology Features

Random Access Dispensing or RAD models offer the most gentle dispensing possible to support sensitive cellular assays. The single-tube cassettes are ideal for reagent preservation, hit-picking or partial plate filling. The 8-to-1 channel bulk ­dispensing cassettes are designed to preserve cell monolayers in low-density plates. An external Peri-pump powers the RAD cassettes, which are not compatible with the internal Peri-pump.
At a glance:
Features Single-tube 8-to-1 tube
Plate Types
Cassette tubing
6- to 384-well 6-, 12-, 24-well
1 µL, 5 µL, or 10 µL 5 µL only
Primary Uses
Example Application
Random dispensing in 48-, 96-, and 384-well plates
Dispensing costly reagent ­lowest dead volume
Fast but gentle dispensing with "Tip Tracking"
Media addition to cells in low-density plates
BioTek Instruments, Inc.
6 | Chapter 1: Introduction
Features Single-tube 8-to-1 tube
Other Hit picking: fast, intuitive
selection of individual wells, rows, or columns; Access and preserve more reagent: single tube can handle minute quantities of reagent.
MultiFlo FXModels
Tip Tracking: gradually raises the tip chute as fluid is dispensed to the well to ensure the least disturbance possible. See RADTip Tracking on
page 156.
cell monolayer is preserved
Model Internal Peri-pump Strip Washer RAD Technology
MFX
MFXW X
MFXP X
MFXPW X X
MFXR X
MFXPR X X
The Syringe and secondary Peri-pump dispensers are ordered separately. Except RAD models include the external Peri-pump.
MultiFlo™ FX Multi-Mode Dispenser
MultiFlo FX Dispenser Comparison | 7

MultiFlo FX Dispenser Comparison

Counting the washer as a potential dispenser, the MultiFlo FX offers three distinct dispensers. Here is a comparison of the devices:
n For precious reagents use the Peri-pump to preserve unused fluids. It has
the shortest, most visible fluid path, and a Purge capability to reverse the fluid flow to recover fluid from the tubing. Another advantage is the ability to dedicate a dispense cassette to use with one reagent only, reducing the amount of priming required prior to use. And, you can shorten the tubing to further reduce the dead volume: See Shorten the Dispense Cassette
Tubing on page 61.
n RAD Technologyoffers the best tools for preserving cells and reagents.
n All MultiFlo FX devices are capable of dispensing up to 30,000 µL. BioTek's
recommended maximum dispense volumes are cited here.
Volume
Device
range µL/well
Peri-pump 0.5‡, and
1-3000*
RAD Technology
0.5‡, and 1­30,000*
Syringe 8-
10-3000 <5% CV @
tube/6-well
Precision Accuracy
<10% CV @ 1 µL/well (typical
+/-10% (typical +/-3%) @ 1 µL/well
<3% CV)
<10% CV @ 1 µL/well (typical
+/-10% (typical +/-3%) @ 1 µL/well
<3% CV)
±2 µL @
20 µL/well
10 µL/well
Approximate Dead volume
Cassette Type:
1 µL 1.20 mL
5 µL 4.23 mL
10 µL 7.36 mL
Type Dead Vol.
1 µL 150 µL
5 µL 530 µL
10 µL 920 µL
For all manifold types: 12 mL
Syringe 16-tube 5-3000 <10% CV
@ 5 µL/well
±2 µL @ 10 µL/well
Syringe 12-/24- 5-30,000 <3% CV @ ±2 µL @
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8 | Chapter 1: Introduction
Volume
Device
/48-well certain
Syringe 32-tube 3-3000 <12% CV
Strip Washer 20 –
*1 µL cassettes' maximum recommended dispense volume is 50 µL/well. ‡ 0.5 µL dispensing is supported when using a 1 µL cassette.
¥Depending on wash manifold, See Performance Specifications on page 21.
range µL/well
30,000
Precision Accuracy
any
µL/well
@ 6 µL/well
≤3.0 - 5.0
¥
% CV
µL/well
±5% @ 6 µL/well
≤±3.0% 12 mL
Approximate Dead volume
BioTek recommends priming a dispenser with three times its dead volume to prepare it for accurate dispensing.
Processing Time
§
Protocols were optimized for speed to obtain the following processing times, including the fastest flow and travel rates. Some of these parameters are listed in the Parameters column of the table. Only standard, non-RAD Peri-pump cassettes are referenced here.
Device Plate
Type
Peri-pump - 5 µL 96 10 High flow rate 3 Peri-pump - 1 µL 384 1 High flow rate 6
1536 1 High flow rate 21 Syringe 8-tube 96 20 Flow rate 1 6.5 Syringe 16-tube 96 20 Flow rate 1 5.25
384 20 Flow rate 1 14 Syringe 32-tube 1536 3 One SB manifold 16.5
1536 14 One LB manifold 27 Strip Washer 96 300 3 cycles <105
Volume (µL/well)
Parameters Time in
seconds
§ Review the Specifications for more details.
¥ Excluding plate carrier and manifold homing movements.
SB = small bore Syringe manifold; LB = large bore manifold.
¥
MultiFlo™ FX Multi-Mode Dispenser
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