Storage in Incubator: How Long Can Cells Be Stored?

  • Thread starter Thread starter Goodie
  • Start date Start date
  • Tags Tags
    Storage
AI Thread Summary
Cells can be stored in an incubator for several days if immediate use is not required, but it's crucial to maintain the culture actively. Regular medium changes depend on the cell type; for instance, PC12 cells need feeding every other day, while Hepa 1C1C7 cells can last up to four days. Monitoring the medium's color using phenol red can indicate when a change is necessary. It's advisable to freeze some cells as a backup to prevent loss due to contamination or other issues, especially if there is no existing frozen stock. Keeping track of passage numbers is important, as cell characteristics may change over time, impacting experimental results.
Goodie
Messages
20
Reaction score
0
i wonder how long can i store my cells in incubator if i don't need the cells right away, but in coming days? should i change the medium regularly when i store the cells in the incubator instead of freezing? or do i have to freeze down the cells immediately and thaw them when i need them?

appreciate for all help.
 
Biology news on Phys.org
Goodie said:
i wonder how long can i store my cells in incubator if i don't need the cells right away, but in coming days? should i change the medium regularly when i store the cells in the incubator instead of freezing?

If it's days you are considering, it's probably best to keep the culture going in the incubator. Split the cultures at a dilution that will allow them to achieve the density you desire on or near the day you plan to use them.

As far as feeding, it usually depends on the cell type, which dictates how metabolically active they are. As an example of cells I've maintained, PC12 cells (from a pheochromocytoma) require feeding every other day, but Hepa 1C1C7 cells (mouse liver) can go about four days between feedings. The state of the culture can also determine how often you feed, thus a fully confluent monolayer might require more frequent feedings than a very lightly populated flask that was just seeded. If you can't find the information on your specific cell type in the literature, your best bet would be to include phenol red in your medium. This indicator will turn from ~cherry red to yellow as the cells metabolize and cast off acidic waste products. If the medium starts to look yellow, it's best to do a medium change.

Goodie said:
do i have to freeze down the cells immediately and thaw them when i need them?

Having said this, if you don't already have a good supply of frozen stocks to work from, it would be best for you to freeze some away for future use, you never know when your cultures might get contaminated and require starting over. Another thing to consider is the passage number, or how many times you have split the cells. Sometimes certain characteristics in a cell line can change as they "age" so keeping track of the passages can aid in limiting/controlling this potential variation. Many researchers will describe passage number used for their experiments so that others are aware of the state of the cells.
appreciate for all help.
 
Thanks alot. :smile:
 
Chagas disease, long considered only a threat abroad, is established in California and the Southern U.S. According to articles in the Los Angeles Times, "Chagas disease, long considered only a threat abroad, is established in California and the Southern U.S.", and "Kissing bugs bring deadly disease to California". LA Times requires a subscription. Related article -...
I am reading Nicholas Wade's book A Troublesome Inheritance. Please let's not make this thread a critique about the merits or demerits of the book. This thread is my attempt to understanding the evidence that Natural Selection in the human genome was recent and regional. On Page 103 of A Troublesome Inheritance, Wade writes the following: "The regional nature of selection was first made evident in a genomewide scan undertaken by Jonathan Pritchard, a population geneticist at the...
Back
Top