NRX1B Polyclonal Antibody, 20ul Subcellular Fractions Mutations in this gene result

Mutations in this gene result in autosomal dominant congenital stationary night blindness

is a 2038 amino acid cytoplasmic protein that contains one protein kinase domain

Sporadic and familial mutations in this gene result in paragangliomas and pheochromocytoma

and found to form heteropentamer swithNP1 andNP2

NRX1B Polyclonal Antibody, 20ul Subcellular Fractions Mutations in this gene resultalternative products: A number of isoforms are produced by alternative promoter usage including the alpha type (shown here) and beta type (AC P58400) isoforms which differ in their N terminus. Additional isoforms may be produced by alternative splicing,alternative products: A number of isoforms, alpha type (AC Q9ULB1) and beta type (shown here), are produced by alternative promoter usage. Beta type isoforms differ from alpha type isoforms in their N