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iPSc with 21 trisomy  
iPSc with 18 trisomy  
iPSc with WFS1` mutation iPS CELLS WITH CHROMOSOME 18 TRISOMY
DESCRIPTION
Trisomy 18, also called Edwards syndrome, is a chromosomal condition associated with abnormalities in many parts of the body. Individuals with trisomy 18 often have slow growth before birth (intrauterine growth retardation) and a low birth weight. Affected individuals may have heart defects and abnormalities of other organs that develop before birth. Other features of trisomy 18 include a small, abnormally shaped head; a small jaw and mouth; and clenched fists with overlapping fingers.
Key hallmarks of iPSc with chromosome 18 trisomy
Key hallmarks of iPSc with chromosome 18 trisomy
- Generated from cells from patients with Edwards Syndrome
- Expressed pluripotent genes
- Exhibited normal proliferation
Molecular markers
TRA1-60 and TRA1-80
TRA1-60 and TRA1-80
Description
Celther Cat. No.:
CLTH/T18 - iPSc
CL 05012-CLTH
APPLICATIONS
Study human 18 trisomy
SPECIFICATIONS
General Specifications
Form:  
Cryopreserved
Format: 
Vial(s)
Species:  
Human
Quantity:  
1 vial
Cell Type:  
Human iPSc derivative, cells generated from cells from patients with Edwards Syndrome
Culture Type:  
Adherent Cell Culture
Donor Source:  
Single Donor
Product Size:  
1 mL
Number of Cells:  
1x106
Tests Performed:  
Sterility Testing (Bacteria & Fungi)
Regulatory Statement:  
For Research Use Only. Not for use in diagnostic procedures.