MOT9 Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Mutations in this gene cause

Mutations in this gene cause the autosomal recessive leukocyte adhesion deficiency syndrome-III (LAD-III)

Several transcripts encoding different isoforms have been found for this gene

p60 (CHAF1B

This intronless gene HSPA1A(heat shock protein family A(Hsp70) member 1A) encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family

Proteasome-mediated degradation of this protein has been shown to be involved in the inactivation of the erythropoietin receptor

MOT9 Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Mutations in this gene causeProton linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates.,Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2. A. 1. 13) family.,