宁波泰斯拓生物

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xrs5

货号 TS210641
中文名称 null
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产品简介
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产品名称: xrs5
商品货号: TS210641
Organism: Cricetulus griseus, hamster, Chinese
Tissue: ovary
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent
Biosafety Level: 1

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.

Gender: female
Applications:
xrs5 is a X-ray sensitive Chinese Hamster Ovary mutant cell line which was derived from CHO-K1 cells by treating the cells with ethyl methanesulphonate and subsequent growth in agar.
Storage Conditions: liquid nitrogen vapor phase
Derivation:
xrs5 is a X-ray sensitive Chinese Hamster Ovary mutant cell line which was derived from CHO-K1 cells by treating the cells with ethyl methanesulphonate and subsequent growth in agar.
Clinical Data:
female
Comments:
xrs5 is a X-ray sensitive Chinese Hamster Ovary mutant cell line which was derived from CHO-K1 cells by treating the cells with ethyl methanesulphonate and subsequent growth in agar.
These cells belong to X-ray complementation group 5 and are mutant in the p86 subunit of the Ku autoantigen.
Ku has been shown to be involved in DNA double-strand break repair and V(D)J recombination.
The cells will revert to wild type on treatment with azacytidine.
Complete Growth Medium: Alpha minimum essential medium without ribonucleosides and deoxyribonucleosides with 2 mM L-glutamine, 90%; fetal bovine serum, 10%
Subculturing: Volumes used in this protocol are for 75 cm2 flask; 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 0.25% (w/v) Trypsin-0.53mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 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).
  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.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: 1:6 to 1:10
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a Manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation:

Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor: G Chu
References:

Jeggo PA, Kemp LM. X-ray-sensitive mutants of Chinese hamster ovary cell line. Isolation and cross-sensitivity to other DNA-damaging agents. Mutat. Res. 112: 313-327, 1983. PubMed: 6197643

Rathmell WK, Chu G. Involvement of the Ku autoantigen in the cellular response to DNA double-strand breaks. Proc. Natl. Acad. Sci. USA 91: 7623-7627, 1994. PubMed: 8052631

Rathmell WK, Chu G. A DNA end-binding factor involved in double-strand break repair and V(D)J recombination. Mol. Cell. Biol. 14: 4741-4748, 1994. PubMed: 7516471

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.