Cellosaurus STF1-169 (CVCL_F744)
Cell line name | STF1-169 |
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Synonyms | STF1.169 |
Accession | CVCL_F744 |
Resource Identification Initiative | To cite this cell line use: STF1-169 (RRID:CVCL_F744) |
Comments | Population: Moroccan. Genetic integration: Method=Transfection/transduction; Gene=UniProtKB; P00557; Escherichia coli hygromycin-B 4-O-kinase (hph) (HygR). Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Sequence variations |
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Disease | Bare lymphocyte syndrome type 1 (NCIt: C171267) Immunodeficiency by defective expression of MHC class I (ORDO: Orphanet_34592) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_A5NE (STF-1) |
Sex of cell | Male |
Age at sampling | 6Y |
Category | Transformed cell line |
Publications | PubMed=17977821; DOI=10.1074/jbc.M708139200 PubMed=18802093; DOI=10.4049/jimmunol.181.7.4894 |
Cross-references | |
Anatomy/cell type resources | BTO; BTO_0003755 |
Encyclopedic resources | Wikidata; Q54970575 |
Entry history | |
Entry creation | 11-Feb-2013 |
Last entry update | 19-Dec-2024 |
Version number | 12 |