Cellosaurus NISK9 (CVCL_LB87)
Cell line name | NISK9 |
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Synonyms | NISK 9 |
Accession | CVCL_LB87 |
Resource Identification Initiative | To cite this cell line use: NISK9 (RRID:CVCL_LB87) |
Comments | Group: Patented cell line. Registration: International Depositary Authority, European Collection of Cell Cultures (ECACC); 09709106. Characteristics: Insulin secreting. Characteristics: Compared to the parent cell line, it has a repaired ATP-regulated potassium channel activity. Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:59; ABCC8. Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:6257; KCNJ11. Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:6107; PDX1. |
Disease | Persistent hyperinsulinemic hypoglycemia of infancy (NCIt: C122923) Autosomal dominant hyperinsulinism due to SUR1 deficiency (ORDO: Orphanet_276575) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_LB86 (NES2Y) |
Category | Spontaneously immortalized cell line |
Publications | PubMed=10567373; DOI=10.1074/jbc.274.48.34059 Patent=US6372501 |
Cross-references | |
Encyclopedic resources | Wikidata; Q54930632 |
Entry history | |
Entry creation | 22-Aug-2017 |
Last entry update | 19-Dec-2024 |
Version number | 8 |