SPI2 Polyclonal Antibody, 100ul Protein Modification and is capable of inducing

and is capable of inducing experimental autoimmune uveoretinitis

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

other named neuronal pentraxin receptor (NPR)

This highly conserved protein family is found in both plants and mammals

Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus| multiple sclerosis and rheumatoid arthritis

SPI2 Polyclonal Antibody, 100ul Protein Modification and is capable of inducingThe 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.