ABCF3 Polyclonal Antibody, 100ul Sampling Tubes Defects in GJC2 are the

Defects in GJC2 are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1

The protein (ankyrin repeat domain 1) encoded by ANKRD1 is localized to the nucleus of endothelial cells and is induced by IL-1 and TNF-alpha stimulation

which bind to one another in a homophilic manner

Although the BCR-ABL fusion protein has been extensively studied

Alternatively spliced transcript variants encoding different isoforms have been found for EIF2B3

ABCF3 Polyclonal Antibody, 100ul Sampling Tubes Defects in GJC2 are theLacks transmembrane domains and is probably not involved in transport. Belongs to the ABC transporter family. EF3 subfamily. Contains 2 ABC transporter domains.