3T3-F442A
70654, mouse adipose tissue, Fibroblast-like
Synonym(e):
3T3F442A Cells, F442A Cells
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About This Item
Empfohlene Produkte
product name
3T3-F442A, 00070654
Biologische Quelle
mouse adipose tissue
Wachstumsmodus
Adherent
Karyotyp
Not specified
Morphologie
Fibroblast-like
Produkte
Not specified
Rezeptoren
Not specified
Methode(n)
cell culture | mammalian: suitable
Versandbedingung
dry ice
Lagertemp.
−196°C
Ursprung der Zelllinie
Mouse pre-adipocytes
Beschreibung der Zelllinie
Cells will differentiate into adipocytes once confluent which takes approximately 10 days. Once confluent, cells should be grown in DMEM and 10% FCS and 5 micrograms/ml insulin. Media changes should take place every 48 h.
To manage customer expectations regarding the potential of 3T3 cell line stocks to differentiate into adipocytes, if using the cells for adipocyte differentiation please note: when cells are stimulated, using an appropriate protocol, differentiation may take several weeks to occur, e.g., 2 - 5 weeks, and the proportion of the population that differentiates can be limited. If 3T3 cells from an alternate source were previously used, we cannot guarantee the differentiation performance will be the same.We are working to source a new stock of this cell line that has a higher rate of adipocyte differentiation potential which we aim to be able to offer in the future. When this is available we will update the cell line details on the website.
To manage customer expectations regarding the potential of 3T3 cell line stocks to differentiate into adipocytes, if using the cells for adipocyte differentiation please note: when cells are stimulated, using an appropriate protocol, differentiation may take several weeks to occur, e.g., 2 - 5 weeks, and the proportion of the population that differentiates can be limited. If 3T3 cells from an alternate source were previously used, we cannot guarantee the differentiation performance will be the same.We are working to source a new stock of this cell line that has a higher rate of adipocyte differentiation potential which we aim to be able to offer in the future. When this is available we will update the cell line details on the website.
Anwendung
Once terminally differentiated the cells can be used as a model for either adipocyte differentiation or mature adipocytes.
Nährmedium
Subkultur-Routine
Split sub-confluent cultures (70-80%) 1:3-1:5 ie. seeding at 2-4 x10,000 cells/cm2 using 0.25% trypsin or trypsin/EDTA, 5% CO2, 37°C. If cells are allowed to become confluent they will differentiate into adipocytes. If cryopreserving these cells, use New
Sonstige Hinweise
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