iPSC Lines - Detail

Designation
T4-32Cr2
Alias
T4 32Cr NKX2.1 Pt 4; T4 32Cr2
Description
hiPSC ChILD NKX2.1 mutant (Brain-Lung-Thyroid Syndrome), Pt 4 c.552_556del5 (CCCGC)
Species Cell Type Disease Ethnicity Race Karyotype Age Parent Avail
Human IPSC Interstitial Lung Disease None Reported None Reported 46XY NR No


 
Institution Boston University
Passage Number PX+27
Starting Materials Dermal Fibroblasts
Culture Platform mTeSR adapted
IPSC Reprogramming Method EF1a-hSTEMCCA4 loxp lentiviral infection
 
 
 
 
File Name Document Type
T4-32Cr2 IF.pdf Immunofluorescence Staining
T4-32Cr2 KT.pdf Karyotype