I did my PhD in the Department of Chemical Engineering at Imperial College London. My research focused on mathematical modeling of the cell cycle in leukemia and involved experiments with cell lines. During that time, I had to count cells with a hemocytometer so often to track growth that I got tired and decided to build an app, HemocyTap, and share my knowledge on the topic here to help as many people as possible.

Having little beasts growing in your cultures is not a good thing – after all, you are studying your cells, not whatever hosts decide to join them… Depending on the contamination, you will observe different anomalies in your culture:

  • Macroscopically: if your medium looks yellow or very cloudy (notice the difference between high-cell-density-cloudiness and contamination-cloudiness; you should see that under the microscope)
  • Microscopically: if you see cells that don’t look like yours, or funny little worms moving around, or aggregates of very small thingies – you have a problem
  • Analytically: because some species are too small (<1μm) to detect under the microscope, there are analytical techniques to test their presence. These include DNA staining, PCR or agar plating (to amplify the numbers).

Comments

Leave a Reply

Your email address will not be published.