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Cellosaurus hIPSC-Di21-C2-4-3 (CVCL_D1FC)

[Text version]
Cell line name hIPSC-Di21-C2-4-3
Synonyms Di C2-4-3; C2-4-3
Accession CVCL_D1FC
Resource Identification Initiative To cite this cell line use: hIPSC-Di21-C2-4-3 (RRID:CVCL_D1FC)
Comments Population: Caucasian.
Characteristics: This cell line has lot one copy of chromosome 21. Using CRISPR/Cas9 a IRES-TK-Neo-polyA site cassette was introduced in one allele of exon 3 of APP on chromosome 21 of the parent cell line. The parent cell line was cultured in the absence of G418 selection for three passages to allow chromosome loss to take place, and then were cultured in the presence of ganciclovir (GCV) to select a clone without the presence of the TK-neo construct (PubMed=23084023).
Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Down syndrome (NCIt: C2993)
Down syndrome (ORDO: Orphanet_870)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_D1F9 (hIPSC-Tri21-C2-4)
Sex of cell Female
Age at sampling 1Y
Category Induced pluripotent stem cell
Publications

PubMed=23084023; DOI=10.1016/j.stem.2012.08.004
Li L.B., Chang K.-H., Wang P.-R., Hirata R.K., Papayannopoulou T., Russell D.W.
Trisomy correction in Down syndrome induced pluripotent stem cells.
Cell Stem Cell 11:615-619(2012)

Cross-references
Cell line collections (Providers) WiCell; hipsc-di21-c2-4-2
Entry history
Entry creation30-Jan-2024
Last entry update30-Jan-2024
Version number1