iPSC Lines - Detail

Designation
BT2
Alias
BT2-1
Description
"compund heterozygous: IVS I-6 T>C ?+-thalassemia mutation; Codon 39 CAG>TAG or Glun39Term ?0-thalassemia mutation."
Species Cell Type Disease Ethnicity Race Karyotype Age Parent Avail
Human IPSC Thalassemia None Reported None Reported 46XY 6 Yes


 
Institution Boston University
Passage Number 14
Starting Materials PBMCs
Culture Platform mTeSR adapted
IPSC Reprogramming Method EF1a-hSTEMCCA4 loxp lentiviral infection
 
 
 
 
File Name Document Type
BT2-1 IF.pdf Immunofluorescence Staining
BT2-1 KT.pdf Karyotype
BT2-1 STR analysis.pdf STR Analysis