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WT SV40 MEF
WT SV40 MEF
規格:
價格:
編號:B190482
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱
WT SV40 MEF
商品貨號
B190482
Organism
Mus musculus, mouse
Tissue
embryonic fibroblast
培養基
Cell Type
fibroblast
Product Format
frozen
Morphology
fibroblast-like
Culture Properties
adherent
Biosafety Level
2

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Applications

This cell line can be paired with MEF cell lines, generated from BCL-2 family member knockout mice (e.g., ATCC CRL-2908, ATCC CRL-2909, ATCC CRL-2910, ATCC CRL-2911, ATCC CRL-2912, ATCC CRL-2913), as a control to study the molecular mechnaisms of cell apoptosis and the BCL-2 family signaling pathway.


Storage Conditions
liquid nitrogen vapor phase
Images
CRL-2907 Micrograph
Derivation

These cells are SV40 immortalized mouse embryonic fibroblasts (MEFs), which were generated from wild type mice.

Tumorigenic
no
Comments

These cells are SV40 immortalized mouse embryonic fibroblasts (MEFs), which were generated from wild type mice.

This cell line can be paired with MEF cell lines, generated from BCL-2 family member knockout mice (e.g., ATCC CRL-2908, ATCC CRL-2909, ATCC CRL-2910, ATCC CRL-2911, ATCC CRL-2912, ATCC CRL-2913), as a control to study the molecular mechnaisms of cell apoptosis and the BCL-2 family signaling pathway.

The cells will slough off of the growth surface if they become too heavy.

Complete Growth Medium
The base medium for this cell line is ATCC-formulated IMDM Catalog No. 30-2005. To make the complete growth medium, add the following components to the base medium: 10 % Fetal Bovine Serum and 1x Non-essential amino acids.
Subculturing
Volumes used in this protocol are for 75 cm2 flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 1.0 to 2.0 mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37.0°C to facilitate dispersal.
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 5 X 103 to 1 X 104 viable cells/cm2 is recommended.
  6. Incubate cultures at 37°C. At subculture, cell concentration is between 1 X 105 to 2 X 105 cells/cm2.

Subcultivation ratio: A subcultivation ratio of 1:8 to 1:20 is recommended.
Medium renewal: Every 2 to 3 days
Cryopreservation
Freeze medium: 90% Fetal Bovine Serum and 10% DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Name of Depositor
S Korsmeyer
References

Wei M, et al. Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death. Science 292(5517): 727-730, 2001 PubMed: 11326099

Lindsten T, et al. The Combined Functions of Proapoptotic Bcl-2 Family Members Bak and Bax Are Essential for Normal Development of Multiple Tissues. Molecular Cell 6(6): 1389-1399, 2000 PubMed: 11163212

Zong WX, et al. BH3-only proteins that bind pro-survival Bcl-2 family members fail to induce apoptosis in the absence of Bax and Bak. Genes Dev. 15(12): 1481-6, 2001 PubMed: 11410528

Cheng EH, et al. BCL-2, BCL-XL Sequester BH3 Domain-Only Molecules Preventing BAX- and BAK-Mediated Mitochondrial Apoptosis. Molecular Cell 8(3) : 705–711, 2001 PubMed: 11583631

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