RGS5 Polyclonal Antibody, 100ul Culture Media Mutations in this gene are

Mutations in this gene are associated with DFNA20/26| a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss

EEF1A1 has been found to have multiple copies on many chromosomes

Splicing factor 3b| together with splicing factor 3a and a 12S RNA unit| forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP)

Acts as a negative regulator of the Toll-like and IL-1R receptor signaling pathways

In the SCF complex

RGS5 Polyclonal Antibody, 100ul Culture Media Mutations in this gene areRGS5 (regulator of G protein signaling 5) encodes a member of the regulators of G protein signaling (RGS) family. The RGS proteins are signal transduction molecules which are involved in the regulation of heterotrimeric G proteins by acting as GTPase activators. RGS5 is a hypoxia inducible factor 1 dependent, hypoxia induced gene which is involved in the induction of endothelial apoptosis. RGS5 is also one of three genes on chromosome 1q contributing