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DiGeorge II/Satellite Enumeration 10 Probe
- Specification
Cat.No.
FMDC-11
Description
DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial (VCFS), share the deletion of chromosome 22 at 22q11. However, deletions on 10p13.14 have been shown in some DGS.
Size
5 Tests, 10 Tests
Label
Red/Green
Specificity
Human
Locus
10p14
Usage
For Research Use Only. Not for use in diagnostic procedures.Storage
Store at minus 20 centigrade
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.
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