Acrosin Polyclonal Antibody, 100ul Erlenmeyer Flasks Mutations in this gene cause

Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I

May function in transmigration of leukocytes through epithelial and endothelial tissues

resulting in the inhibition of TRAF6 NF-kappa-B activation

subcellular location:Associated with the endoplasmic reticulum and nuclear

fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots

Acrosin Polyclonal Antibody, 100ul Erlenmeyer Flasks Mutations in this gene causeAcrosin is the major proteinase present in the acrosome of mature spermatozoa. It is a typical serine proteinase with trypsin like specificity. It is stored in the acrosome in its precursor form, proacrosin. The active enzyme functions in the lysis of the zona pellucida, thus facilitating penetration of the sperm through the innermost glycoprotein layers of the ovum. The mRNA for proacrosin is synthesized only in the postmeiotic stages of