USER GUIDE
CTS™ TrypLE™ Select
Catalog Numbers A4738001 and A1285901
Pub. No. MAN0007390 Rev. 2.0
WARNING! Read the Safety Data Sheets (SDSs) and follow the handling instructions. Wear appropriate protective eyewear,
clothing, and gloves. Safety Data Sheets (SDSs) are available from thermofisher.com/support.
Product description
TrypLE™, an animal origin-free alternative to porcine trypsin, is a recombinant enzyme derived from microbial fermentation. TrypLE
is used for the dissociation of attachment-dependent cell lines from plasticware. TrypLE™ has demonstrated ability to dissociate cells
cultured both in serum-free and serum-supplemented systems. The Gibco™ CTS™ product line enables you to reduce your burden in
qualifying reagents during your transition from research applications to clinical applications.
Contents and storage
™
Product Catalog No. Amount Storage Shelf Life
CTS™ TrypLE™ Select (Bag) A4738001 1 L 15°C to 30°C
Protect from light
CTS™ TrypLE™ Select (Bottle) A1285901 100 mL 15°C to 30°C
Protect from light
[1]
Shelf Life duration is determined from Date of Manufacture.
5.
Procedural guidelines
• Formulated in DPBS with 1 mM EDTA.
• Substitutes directly into existing protocols.
• No inactivation required; dilution alone inactivates TrypLE
avoiding the need for trypsin inhibitors.
Detach cells
TrypLE™ is designed as a direct substitute for trypsin in existing
protocols. Optimal conditions and concentrations employed for
individual systems should be determined empirically.
1. Prewarm TrypLE™ and complete growth medium to 37°C
before use. Minimize dwell time.
Note: TrypLE™ may be used at ambient room temperature for
many types of cells.
™
Incubate at 37°C until cells have detached. Observe cell
monolayer using an inverted microscope to ensure complete
cell detachment from the surface of the flask. Gently tap
flask to dislodge cells.
6. Add 5–10 mL of complete medium to the flask. Tilt the flask
in all directions to thoroughly rinse the flask. Transfer the cell
suspension to a 15‑mL conical tube.
7. Centrifuge at 100 × g for 5–10 minutes.
8. Discard supernatant and resuspend the cell pellet in 2–5 mL
of complete medium.
9. Determine the viable density using a Countess™ Automated
Cell Counter or alternative automated or manual method.
10. Seed, incubate, and subculture according to normal
protocols depending on your cell type.
[1]
12 months
24 months
2. Aspirate spent medium and discard.
3. Wash cell monolayer with 5 mL of prewarmed CTS
Dulbecco’s Phosphate Buered Saline (DPBS) without
calcium and magnesium. Aspirate and discard.
4. Add an appropriate volume (e.g., 5 mL in a 75 cm2 flask)
of TrypLE™ to the flask. Ensure complete coverage of cell
monolayer with TrypLE™.
™
Note: Use of soybean trypsin inhibitor is not recommended.
For Research Use or Manufacturing of Cell, Gene, or Tissue- Based Products. CAUTION: Not
intended for direct administration into humans or animals.
Related products
Product Catalog No.
CTS™ Dulbeccos Phosphate Buered Saline (DPBS)
A12856
without calcium, magnesium, or phenol red (1X),
Liquid
UltraPure™ 0.5 M EDTA, pH8.0 15575
Water, distilled 15230
Trypan Blue Stain 15250
Countess™ Automated Cell Counter C10227
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The information in this guide is subject to change without notice.
DISCLAIMER: TO THE EXTENT ALLOWED BY LAW, THERMO FISHER SCIENTIFIC INC. AND/OR ITS AFFILIATE(S) WILL NOT BE LIABLE FOR SPECIAL, INCIDENTAL, INDIRECT,
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Revision history: Pub. No. MAN0007390
Revision Date Description
2.0 05 March 2021 Rebranded. Added sku A4738001.
1.0 2012 New document.
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applicable Limited Use Label Licenses.
Limited Use Label License No. 517: Internal Research and Bioproduction Use: Notice to Purchaser: The purchase of this product conveys to the purchaser the limited, nontransferable right to use the purchased amount of the product to (a) perform internal research for the sole benefit of the purchaser; (b) manufacture protein (or other biological material)
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may transfer this product, its components, or materials made using this product to a third party (including contract research/manufacturing organizations), provided that each such third
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product in any form; (2) use the product as a therapeutic agent or diagnostics test component; (3) reverse engineer the product or cause the product to be reverse engineered; or (4)
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