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

It encodes a ubiquitous cytosolic phosphoprotein proposed to function as an intracellular relay integrating regulatory signals of the cellular environment

MRPS17 (mitochondrial ribosomal protein S17) encodes a 28S subunit protein that belongs to the ribosomal protein S17P family

and a motif homologous to one identified in signaling lymphocyte activation molecule (SLAM

Although the BCR-ABL fusion protein has been extensively studied

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.