SPI2 Polyclonal Antibody, 100ul Protein Modification Defects in this gene are

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

and is capable of inducing experimental autoimmune uveoretinitis

The protein encoded by this gene belongs to the phosphatase 2A regulatory subunit B family

while the re-sealable bag keeps them safe and organized

SPI2 Polyclonal Antibody, 100ul Protein Modification Defects in this gene areThe 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.