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iPS cells | Turner Syndrome Derived iPSc
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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.

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