KURB1889 CS2AW

Cell information

Cell type：human mutant cell repository from Kyoto University (View Pricing Information)

JCRB No.   KURB1889 Cell Name   CS2AW
Profile   Hereditary disease showing accelerated aging Cockayne syndrome, group(A), (autosomal recessive) skin fibroblast, high sensitivity to UV. Other Name   
Animal   human Strain   
Genus   Homo Species   sapiens
Sex   F Age   5Y
Identity    Tissue for Primary Cancer   skin
Case history   Cockayne syndrome (A) Metastasis   
Tissue Metastasized    Genetics   Group A Cockayne syndrome cells without XP phenotype.
Life Span    Crisis PDL   
Morphology   fibroblast-like Character   skin fibroblast
Classify   primary Established by   Ikenaga M.
Registered by   Radiation Biology Center, Kyoto University Regulation for Distribution   
Comment   sister of CS1AW same as JCRB0310 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

Link
Cellosaurus(ExPASy) Cellosaurus (ExPASy) is developed by Amos Bairoch of the CALIPHO group at the SIB - Swiss Institute of Bioinformatics as part of the neXtProt project. Cellosaurus is a knowledge database of cell lines with various information summarized. CVCL_2879
Reference
Pubmed id:noneCockayne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

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