SPI2 Polyclonal Antibody, 20ul Lentiviral Packaging The chromosome 22 breakpoint for

The chromosome 22 breakpoint for this translocation is located within the BCR gene (BCR

and functions as a receptor for angiotensin II

Mutations in this gene cause autosomal-recessive intellectual disability

There is no additional adjustment needed

SPI2 Polyclonal Antibody, 20ul Lentiviral Packaging The chromosome 22 breakpoint forThe gene encodes a member of a family of proteins that acts as inhibitors of serine proteases. These proteins function in the regulation of a variety of physiological processes, including coagulation, fibrinolysis, development, malignancy, and inflammation. Expression of the encoded protein may be downregulated during pancreatic carcinogenesis. Alternative splicing results in multiple transcript variants for this gene.