ST2A1 Polyclonal Antibody, 100ul[BT-AP14510] Recombinant Protein and renal and muscular defects

and renal and muscular defects

the polymerase responsible for synthesizing transfer and small ribosomal RNAs in eukaryotes

This gene and family member ABCC12 are determined to be derived by duplication and are both localized to chromosome 16q12

Defects in this gene cause congenital erythropoietic porphyria (Gunther's disease)

ST2A1 Polyclonal Antibody, 100ul[BT-AP14510] Recombinant Protein and renal and muscular defectsThis gene encodes a member of the sulfotransferase family. Sulfotransferases aid in the metabolism of drugs and endogenous compounds by converting these substances into more hydrophilic water soluble sulfate conjugates that can be easily excreted. This protein catalyzes the sulfation of steroids and bile acids in the liver and adrenal glands, and may have a role in the inherited adrenal androgen excess in women with polycystic ovary syndrome.