iPSC Lines - Detail

Designation
SS49
Alias
SS49-1
Description
A>T mutation in beta globin gene
Species Cell Type Disease Ethnicity Race Secondary Race Karyotype Age Parent Avail
Human IPSC Sickle Cell Disease None Reported Black or African American ND 31 No


 
Institution Boston University
Passage Number
Starting Materials PBMCs
Culture Platform mTeSR adapted
IPSC Reprogramming Method EF1a-hSTEMCCA4 loxp lentiviral infection