Ezrin(Phospho Tyr478) Polyclonal Antibody, 20ul Yeast Expression Defects in this gene are

Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN)

Suppression of tumorigenicity 5 protein encoded by ST5 contains a C-terminal region that shares similarity with the Rab 3 family of small GTP binding proteins

This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ)

Mammalian mitochondrial ribosomal protein L 24 (39S ribosomal protein L24 mitochondrial) is encoded by nuclear gene MRPL24 and help in protein synthesis within the mitochondrion

RPS20 (ribosomal protein S20) encodes a ribosomal protein that is a component of the 40S subunit

Ezrin(Phospho Tyr478) Polyclonal Antibody, 20ul Yeast Expression Defects in this gene areThe cytoplasmic peripheral membrane protein encoded by this gene functions as a protein tyrosine kinase substrate in microvilli. As a member of the ERM protein family, this protein serves as an intermediate between the plasma membrane and the actin cytoskeleton. This protein plays a key role in cell surface structure adhesion, migration and organization, and it has been implicated in various human cancers. A pseudogene located on chromosome 3 has been