KURB1403 AP22P
Cell information
Cell type：human mutant cell repository from Kyoto University (View Pricing Information)
| JCRB No. | KURB1403 | Cell Name | AP22P |
|---|---|---|---|
| Profile | Hereditary disease with high cancer risk Fanconi anemia (autosomal recessive), chromosomal breakage syndrome, high sensitivity to mitomycin C (lymphocyte) | Other Name | |
| Animal | human | Strain | |
| Genus | Homo | Species | sapiens |
| Sex | F | Age | 7 |
| Identity | Tissue for Primary Cancer | ||
| Case history | Fanconi anemia (A) | Metastasis | |
| Tissue Metastasized | Genetics | MMC sensitive(lymphocyte), FANCA mutation, karyotype=46,XX (lymphocyte) | |
| Life Span | finite | Crisis PDL | |
| Morphology | fibroblast-like | Character | skin fibroblast |
| Classify | primary | Established by | Sasaki M. |
| 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 | ||||||
| Images |
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