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Gibco™ Versene Solution

Description
- Gibco Versene Solution 0.48 mM
- Formulated as 0.2 g EDTA(Na4) per liter of Phosphate Buffered Saline (PBS)
- Sustainable packaging
Cell Culture, Mammalian Cell Culture
Order Info
Shipping Condition: Room Temperature
Specifications
Specifications
| Chelators | EDTA |
| Content And Storage | Storage conditions: 2 to 8°C Shipping conditions: Ambient Shelf life: 18 months from date of manufacture |
| Classification | Animal Origin-free |
| Product Type | Cell Culture Dissociation Reagent |
| Sterility | Sterile-filtered |
| With Additives | EDTA |
| Manufacturing Quality | cGMP for medical devices, 21 CFR Part 820 and ISO 13485 |
| Quantity | 100 mL |
| Shipping Condition | Room Temperature |
Frequently Asked Questions (FAQs)
Yes. Following 2 passages on the rhLaminin-521 matrix, Versene or EDTA passaging should be used to subculture PSCs.
Here are three major differences to be taken into consideration when culturing cells
in Gibco Essential 8 Medium on Gibco Vitronectin (VTN-N) compared to other feeder-free
systems:
- Cells should be typically passaged ~24 hours sooner than they would be with other feeder-free
media.
- Passaging should take place when cells are at ~85% confluency. If cells are passaged when they
are more than 85% confluent, the health of the cells and final cell yield may be compromised.
- Cells must be passaged in EDTA. Collagenase and dispase are not recommended.
Cells cultured in other feeder-free media systems, such as mTeSR Medium with Matrigel Basement Membrane Matrix, or StemPro hESC SFM with Geltrex Matrix, can be successfully cultured in Gibco Essential 8 Medium and VTN-N. In addition, PSCs grown on feeders with KnockOut SR have also been shown to be successfully cultured in Gibco Essential 8 Medium on VTN-N. However, when changing media systems, cells must be passaged either manually, or with EDTA prior to culturing in Gibco Essential 8 Medium on VTN-N.
Cells cultured in Gibco Essential 8 Medium and VTN-N need to be passaged with EDTA.
This transition is very straightforward. We recommend at least a 2-passage transition into the StemFlex Medium system. Briefly, if you have cryopreserved cells previously cultured in the mTeSR1/Matrigel system, we recommend thawing the cells back into mTeSR1/Matrigel until fully recovered. Upon reaching ~70-85% confluency, passage using Versene solution and seed directly into the StemFlex Medium system.
For Research Use Only. Not for use in diagnostic procedures.
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