HeLa Cell Counts for 100% Confluent Plates

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SUMMARY

The discussion centers on estimating the number of HeLa cells on a 100% confluent 100mm plate, with estimates ranging from 750,000 to 2 million cells based on density. Participants emphasize the variability in cell counts due to factors such as passage number and growth conditions. Reliable counts can only be achieved through direct counting methods, either manually using a microscope or utilizing computer programs designed for pixel counting. Regular examination of plates is recommended to detect potential contamination.

PREREQUISITES
  • Understanding of HeLa cell culture techniques
  • Familiarity with cell confluency concepts
  • Knowledge of microscopy and cell counting methods
  • Experience with image analysis software for cell counting
NEXT STEPS
  • Research HeLa cell culture best practices
  • Learn about manual cell counting techniques using microscopy
  • Explore software options for automated cell counting
  • Investigate factors affecting cell growth and confluency
USEFUL FOR

This discussion is beneficial for cell biologists, laboratory technicians, and researchers involved in cell culture and analysis, particularly those working with HeLa cells and interested in accurate cell counting methodologies.

eab
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i was just wondering if anybody out there had a good guess as to how many HeLa cells were on a 100% confluent, say, 100mm plate (any size would do). my guess would be between 750,000 to 2 million? depending on how dense they get. what would you think 70% would be? does anyone have any numbers for plates this confluency that were counted/sorted?
 
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eab said:
i was just wondering if anybody out there had a good guess as to how many HeLa cells were on a 100% confluent, say, 100mm plate (any size would do). my guess would be between 750,000 to 2 million? depending on how dense they get. what would you think 70% would be? does anyone have any numbers for plates this confluency that were counted/sorted?

there is no way to give a reliable number.

there is just too much variation between cell lines (even if they are all HeLa cells), how many times the cells have been passaged, and your particular growth conditions.

you just have to get down and dirty and count them. you can do it the traditional way with a foot tapper and microscope, or there are computer programs that will count pixels for you.

if you are suspecting contamination, it should be evident if you examine the plates daily.
 

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