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微信小章| 产品名称： | WI-26 VA4 |
|---|---|
| 商品货号： | TS161169 |
| Organism： | Homo sapiens, human |
| Tissue： | lung |
| Cell Type： | SV40 transformed |
| Product Format： | frozen |
| Morphology： | epithelial-like |
| Culture Properties： | adherent |
| Biosafety Level： | 2 Cells contain polyomavirus 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. |
| Age： | 3 month gestation |
| Gender： | male |
| Ethnicity： | Caucasian |
| Applications： | The cells are positive for SV40 neo (T) antigen and SV40 transplantation antigen. |
| Storage Conditions： | liquid nitrogen vapor temperature |
| Karyotype： | Chromosome Frequency Distribution 49 Cells: 2n = 46 Karyotype unstable within triploid stemline range of 67 to 71. Ninety-six percent of the cells have a large chromosome with a submedian centromere. Approximately 52% of the cells have one or more secondary constrictions; 42% of the cells examined had breaks. |
| Derivation： | WI-26 VA4 is an SV40 virus transformed derivative of WI-26 a human diploid fibroblast cell line from embryonic lung tissue. After initial infection and crisis-phase of SV40-transformation, the cells underwent a change in morphology. The cells are positive for SV40 neo (T) antigen and SV40 transplantation antigen. |
| Clinical Data： | male Caucasian 3 month gestation |
| Comments： | WI-26 VA4 is an SV40 virus transformed derivative of WI-26 a human diploid fibroblast cell line from embryonic lung tissue. After initial infection and crisis-phase of SV40-transformation, the cells underwent a change in morphology. The cells are positive for SV40 neo (T) antigen and SV40 transplantation antigen. |
| Complete Growth Medium： | The base medium for this cell line is ATCC-formulated Eagles Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
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| 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.
Subcultivation Ratio: 1:2 to 1:5 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: 5% Carbon dioxide (CO2) |
| STR Profile： | Amelogenin: X,Y CSF1PO: 10,11 D13S317: 12 D16S539: 9,11 D5S818: 11,12 D7S820: 10,13 THO1: 6,7 TPOX: 10,11 vWA: 17,20 |
| Isoenzymes： | G6PD, B |
| Name of Depositor： | AJ Girardi |
| Deposited As： | Homo sapiens |
| References： | Hayflick L, Moorhead PS. The serial cultivation of human diploid cell strains. Exp. Cell Res. 25: 585-621, 1961. PubMed: 13905659 Hayflick L. The limited in vitro lifetime of human diploid cell strains. Exp. Cell Res. 37: 614-636, 1965. PubMed: 14315085 Girardi AJ, et al. SV40-induced transformation of human diploid cells: crisis and recovery. J. Cell. Comp. Physiol. 65: 69-84, 1965. Jensen F, et al. Autologous and homologous implantation of human cells transformed in vitro by simian virus 40. J. Natl. Cancer Inst. 32: 917-937, 1964. 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. Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC. |