MilliporeSigma
All Photos(1)

3T3-F442A

00070654

Synonym(s):
3T3F442A Cells, F442A Cells

biological source

mouse adipose tissue

growth mode

Adherent

karyotype

Not specified

morphology

Fibroblast-like

products

Not specified

receptors

Not specified

technique(s)

cell culture | mammalian: suitable

shipped in

dry ice

storage temp.

−196°C

Related Categories

Compare Similar Items

View Full Comparison

1 of 4

This Item
CB_99072803CB_91060547CB_89062107
3T3-F442A 00070654

3T3-F442A

F5-5.F1 99072803

F5-5.F1

36F Reactivity: Anti-CD2, ovine, 91060547

36F

F15-42-1-5 89062107, Reactivity: Anti-Thy-1, human

F15-42-1-5

biological source

mouse adipose tissue

biological source

mouse spleen

biological source

Mouse x Mouse Hybridoma

biological source

Mouse x Mouse Hybridoma

growth mode

Adherent

growth mode

Suspension

growth mode

-

growth mode

-

karyotype

Adherent

karyotype

Suspension

karyotype

-

karyotype

-

morphology

Adherent

morphology

Suspension

morphology

-

morphology

-

products

Adherent

products

Suspension

products

-

products

-

receptors

Adherent

receptors

Suspension

receptors

-

receptors

-

Cell Line Origin

Mouse pre-adipocytes

Cell Line Description

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.

Application

Once terminally differentiated the cells can be used as a model for either adipocyte differentiation or mature adipocytes.

Subculture 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

Other Notes

Additional freight & handling charges may be applicable for Asia-Pacific shipments. Please check with your local Customer Service representative for more information.

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service