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Cellosaurus RCNSi002-B (CVCL_A1WT)

[Text version]
Cell line name RCNSi002-B
Synonyms HU-DM2-B-2
Accession CVCL_A1WT
Resource Identification Initiative To cite this cell line use: RCNSi002-B (RRID:CVCL_A1WT)
Comments From: RCNS-Institute of Enzymology; Budapest; Hungary.
Population: Caucasian.
Donor information: Established from monozygotic twin of RCNSi001-A (Cellosaurus=CVCL_A1WQ) and RCNSi001-B (Cellosaurus=CVCL_A1WR).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Type 2 diabetes mellitus (NCIt: C26747)
Rare diabetes mellitus type 2 (ORDO: Orphanet_181376)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A1WS ! RCNSi002-A
Sex of cell Female
Age at sampling 66Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=33099106

Markers:
AmelogeninX
CSF1PO10,12
D5S81812,13
D7S8208,11
D13S31711,14
D16S53913
D21S1128,31.2
TH019.3
TPOX8,10
vWA17,18

Run an STR similarity search on this cell line
Publications

PubMed=33099106; DOI=10.1016/j.scr.2020.102051
Szabo E., Ree D., Jezso B., Vincze K., Foldes G., Molnar A.A., Rethelyi J.M., Apati A.
Generation of iPSC lines from peripheral blood mononuclear cells of identical twins both suffering from type 2 diabetes mellitus and one of them additionally diagnosed with atherosclerosis.
Stem Cell Res. 49:102051-102051(2020)

Cross-references
Cell line databases/resources hPSCreg; RCNSi002-B
Encyclopedic resources Wikidata; Q105510751
Entry history
Entry creation12-Jan-2021
Last entry update29-Jun-2023
Version number5