KURB1469 FA17P(SVT)
Cell information
Cell type：human mutant cell repository from Kyoto University (View Pricing Information)
| JCRB No. | KURB1469 | Cell Name | FA17P(SVT) |
|---|---|---|---|
| Profile | Hereditary disease with high cancer risk Fanconi anemia (autosomal recessive), chromosomal breakage syndrom,e high sensitivity to mitomycin C | Other Name | |
| Animal | human | Strain | |
| Genus | Homo | Species | sapiens |
| Sex | M | Age | 11 |
| Identity | Tissue for Primary Cancer | ||
| Case history | Fanconi anemia (G) | Metastasis | |
| Tissue Metastasized | Genetics | MMC sensitive(lymphocyte), FANCG mutation | |
| Life Span | infinite | Crisis PDL | |
| Morphology | fibroblast-like | Character | SV40 Ori-Transfection |
| Classify | transformed | Established by | |
| Registered by | Radiation Biology Center, Kyoto University | Regulation for Distribution | |
| Comment | Year | ||
| Medium | Methods for Passages | ||
| Cell Number on Passage | Race | Japanese | |
| CO2 Conc. | 5% | Tissue Sampling | skin |
| Tissue Type |
| Detection of virus genome fragment by Real-time PCR | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Detected DNA Virus | not tested | Detected RNA Virus | not tested | ||||||