iPSC Lines - Detail

Designation
BR-SP-31
Alias
BR-SP-31-2
Description
A>T mutation in beta globin gene, abnormal KT
Species Cell Type Disease Ethnicity Race Karyotype Age Parent Avail
Human IPSC Sickle Cell Disease None Reported None Reported 46XY 35 Yes


 
Institution Boston University
Passage Number
Starting Materials PBMCs
Culture Platform mTeSR adapted
IPSC Reprogramming Method EF1a-hSTEMCCA4 loxp lentiviral infection
 
 
 
 
File Name Document Type
BR-SP-31-2 KT.pdf Karyotype
BR-SP-31-2 STR Analysis.pdf STR Analysis