宁波泰斯拓生物

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Bak KO SV40 MEF

货号 TS155094
中文名称 null
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产品名称: Bak KO SV40 MEF
商品货号: TS155094
Organism: Mus musculus, mouse
Tissue: embryonic fibroblast
Cell Type: fibroblast
Product Format: frozen
Morphology: fibroblast-like
Culture Properties: adherent
Biosafety Level: 2 xa0 Cells contain SV40 viral DNA sequences

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 is useful to study molecular mechanism of cell apoptosis, BCL-2 family pathway, BAK function, as well as cells that are resistant to multiple apoptotic stimuli.
Storage Conditions: liquid nitrogen vapor phase
Images: CRL-2912 Micrograph
Derivation:

Cells are immortalized MEFs, which were generated from BAK knockout mice.

Tumorigenic: no
Comments:

Cells are immortalized MEFs (genotype: bak-/-), which were generated from BAK knockout mice.

Cells are sensitive to tBID-induced cytochrome c release and apoptosis.

Cells are sensitive to multiple apoptotic stimuli that act through disruption of mitochondrial function: staurosporine, ultraviolet radiation, growth factor deprivation, etoposide, and the endoplasmic reticulum stress stimuli thapsigargin and tunicamycin.xa0

Cells are sensitive to Bim and Bad expression induced apoptosis.

BAK is a pro-apoptotic BCL-2 family member.

This cell line is useful for studying molecular mechanism of cell apoptosis, BCL-2 family pathway, BAK function, as well as cells that are resistant to multiple apoptotic stimuli.

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 Dulbeccos 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°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 7 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.
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: Stanley 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