I haven’t seen a question yet on cell line contamination, i.e. the cells don’t have the correct lineage. What are your thoughts on how to deal with this problem?
This question is part of the following Ask The Expert session:
How to minimize contamination risk and protect your cultures
Answered by:
Company: Corning
Job Title: Scientific Supporting Specialist supporting EMEA regions
Answer
Cross-contamination of cultures is the unintended mix up of different cell lines leading to a mixed population . It can have various causes as example: cross-use or sharing of media from a different cell line, and share Equipment (Biosafety cabinets).
Approaches :
- Quarantine all cultures coming into the laboratory until they have been tested/checked first. A first step when starting a culture is cell authentication to determine identity and species of cells
- Periodically check your cells for morphology or genetic changes. Cell authentication to determine identity and species of cells is extremely important
- Work with only one cell line at a time whenever possible
- Thoroughly clean before and after introducing a new cell line into the laminar flow hood
- Daily cleaning of hood space with 70% alcohol, as well as monthly cleaning with 10% bleach or equivalent products
- Storing cell line stocks in vapor phase of LN2 , not in liquid phase
Ref: CLS-CG-TS-077 REV1 https://www.corning.com/catalog/cls/documents/application-notes/CLS-CG-TS-077.pdf
Please also see – A guide to contamination, which can be a helpful resource as well: https://www.corning.com/