S22A4 Polyclonal Antibody, 20ul Bottle-Top Dispenser Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates| and may lead to Zellweger syndrome| severe mental retardation| and death in children

a motif known to be involved in protein-protein interactions

Most lipocalins are clustered on the long arm of chromosome 9

Alternative splicing results in the multiple transcript variants

The Fos gene family consists of 4 members: fOS

S22A4 Polyclonal Antibody, 20ul Bottle-Top Dispenser Deficiency of this enzyme resultsPolyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is an organic cation transporter and plasma integral membrane protein containing eleven putative transmembrane domains as well as a nucleotide binding site motif. Transport by this protein is at least partially ATP