HSP A5 Polyclonal Antibody, 20ul Vessels Mutations in this gene cause

Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ADAMTS12 (ADAM metallopeptidase with thrombospondin type 1 motif 12) encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family

which is necessary for osmolytic pore formation

FZD8 is highly expressed in two human cancer cell lines

The ITI family contains multiple proteins made up of a light chain (see MIM 176870) and a variable number of heavy chains (Salier et al

HSP A5 Polyclonal Antibody, 20ul Vessels Mutations in this gene cause78 kDa glucose regulated protein encoded by HSPA5 is a member of the heat shock protein 70 (HSP70) family. It is localized in the lumen of the endoplasmic reticulum (ER), and is involved in the folding and assembly of proteins in the ER. As this protein interacts with many ER proteins, it may play a key role in monitoring protein transport through the cell.