You are here PRODUCTS >> CELL LINES >> iPSc & iPSc DERIVATIVES >> TURNER SYNDROME DERIVED iPSc
PRODUCTS
 
Modified cell lines  
iPSc & iPSc derivates  
iPS cells  
iNS cells  
Cardiomyocytes  
Astrocytes  
Neurons  
Hepatocytes  
Celther Endoderm Cells  
Fibroblasts  
iPSc with 21 trisomy  
iPSc with 18 trisomy  
iPSc with WFS1 mutation  
iNSc-IDH1-WT  
iNSc-IDH1- R132H  
iPSc-EGFRvIII  
Cancer-Derived iPSc  
iPSc-derived endoderm  
Turner Syndrome  
Naive cells  
Adult human cells iPSc from patient diagnosed with Izochromosome X
X isochromosome (iso(Xq)) is one of the causes of Turner Syndrome, which is characterized by short stature and loss of ovarian function. This condition affects 1 in 2500-3000 born girls. Additionally, isochromosome X may be associated with predisposition to autoimmune diseases such as Hashimoto’s thyroiditis, celiac disease, Crohn’s disease and other. iPSC generated from cells obtained from patient with iso(Xq) may serve as an in vitro disease model due to their ability to differentiate into cells of thyroid, intestine and others.
Cell line
Celther Cat. No.:
CLTH/iPSc-Xizochromosome
CL 05016 - CLTH
General Specifications
Form:  
Frozen
Format: 
Vial(s)
Species:  
Human
Culture Type:  
Adherent Cell Culture
Donor Source:  
Single Donor
Number of Cells:  
30 colonies
Tests Performed:  
Sterility Testing (Bacteria & Fungi)
Regulatory Statement:  
For Research Use Only. Not for use in diagnostic procedures.