KURB1896 CS1AW(SV)
Cell information
Cell type:human mutant cell repository from Kyoto University (View Pricing Information)
JCRB No. | KURB1896 | Cell Name | CS1AW(SV) |
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Profile | SV40 transformed human fibroblast, Hereditary disease showing accelerated aging (autosomal recessive), Cockayne syndrome, group(A) | Other Name | |
Animal | human | Strain | |
Genus | Homo | Species | sapiens |
Sex | F | Age | 7Y |
Identity | Tissue for Primary Cancer | skin | |
Case history | Cockayne syndrome, group(A) | Metastasis | |
Tissue Metastasized | Genetics | ||
Life Span | Crisis PDL | ||
Morphology | fibroblast-like | Character | SV40 (pkM8-16) Ori-transform |
Classify | transformed | Established by | |
Registered by | Radiation Biology Center, Kyoto University | Regulation for Distribution | |
Comment | sister of CS2AW | Year | |
Medium | Methods for Passages | ||
Cell Number on Passage | Race | Japanese | |
CO2 Conc. | Tissue Sampling | skin | |
Tissue Type |
Detection of virus genome fragment by Real-time PCR | |||||||||
---|---|---|---|---|---|---|---|---|---|
Detected DNA Virus | not tested | Detected RNA Virus | not tested |
Reference | |
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Pubmed id:none | Cockayne症候群:姉妹例の報告と本邦における文献的展望 徳島大学医学部小児科:橋本俊顕ら 脳と発達 10(6):465-472,1978 |