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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
Eszter Szabo, Dora Ree, Balint Jezso, Katalin Vincze, Gabor Foldes, Andrea A. Molnar, Janos M. Rethelyi, Agota Apati;
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