ZPBP1 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Evidence indicates that mutations in

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

Mutations in this gene have been associated with hypertriglyceridemia and hyperlipoproteinemia type 5

Nagashima type

4 N-acetylgalactosaminyltransferase 1 catalyzes the transfer of GalNAc into G(M3) and G(D3) by a beta-1

Interacts with GSK3B

ZPBP1 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Evidence indicates that mutations inZPBP is one of several proteins that are thought to participate in secondary binding between acrosome reacted sperm and the egg specific extracellular matrix the zona pellucida (McLeskey et al. 1998