RS24 Polyclonal Antibody, 100ul Deep Well Plates Defects in this gene cause

Defects in this gene cause Niemann-Pick type C disease| a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments

Product dimensions conform to SBS standards

This family member is part of the MRP subfamily

The encoded protein transports taurine and beta-alanine

This protease is ATP-dependent and targets specific proteins for degradation

RS24 Polyclonal Antibody, 100ul Deep Well Plates Defects in this gene causeRibosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S24E family of ribosomal proteins. It is located in the cytoplasm. Multiple transcript variants encoding different isoforms have