RUO - FP308 Chromosome 10 centromere probe reagent

Cat.# FP-308: Chromosome 10 Centromere Probe Reagent

[Overview]

Chromosome 10 deletion is a chromosome abnormality that occurs when there is a missing copy of genetic material on the long arm (q) or short arm (p) of chromosome 10. The severity and the signs and symptoms depend on the size and location of the deletion, and which genes are involved. Features may affect many parts of the body and may include low birth weight, growth delay, developmental delay, low muscle tone (hypotonia), and communication difficulties. Birth defects, various medical problems, and/or distinctive facial features may also be present.

 

[Download] Chromosome 10 centromere probe reagent

[Download MSDS] MSDS