Q:
A:
35
How do you strain cells?
1. Remove flasks from incubator. Inspect flasks for clumping that
would mandate straining (compare to provided video).
2. Use a fresh, sterile 250 mL shake flask. Remove cap (while
maintaining sterility) and place a sterile cell strainer in the top of
the flask.
3. Pipet or pour culture over strainer.
4. Discard cell strainer and replace cap. Proceed with cell counting
and passage.
For more detailed information, please see the "Thawing and
Subculturing CHO-S
®
Cells (cGMP-banked)" section of the User Guide.
Info:
FAQ Sections
Life Technologies
™
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®
CHO-S
®
Kit FAQ
