RBP Rabbit Polyclonal Antibody, 50ul Tubes Mutations in this gene are

Mutations in this gene are associated with infantile-onset multisystem autoimmune disease and hyper

which encodes a structurally unrelated protein - Alex

Endophilin B1 is a member of the B subgroup of the Endophilin family that is required for maintenance of mitochondrial morphology and for the regulation of the outer mitochondrial membrane dynamics

FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion| both of which are characterized by conserved histidine motifs

and processing of melanocyte protein PMEL

RBP Rabbit Polyclonal Antibody, 50ul Tubes Mutations in this gene areThis protein belongs to the lipocalin family and is the specific carrier for retinol (vitamin A alcohol) in the blood. It delivers retinol from the liver stores to the peripheral tissues. In plasma the RBP retinol complex interacts with transthyretin which prevents its loss by filtration through the kidney glomeruli. A deficiency of vitamin A blocks secretion of the binding protein posttranslationally and results in defective delivery and supply to