P4HA1 Rabbit Polyclonal Antibody, 50ul 3D Culture Mutations of this gene cause

Mutations of this gene cause carboxylesterase 1 deficiency

Contains 1 DEP domain

This gene encodes a protein that belongs to a subfamily of calcium binding proteins which share similarity to calmodulin

This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa

P4HA1 Rabbit Polyclonal Antibody, 50ul 3D Culture Mutations of this gene causeThis gene encodes a component of prolyl 4 hydroxylase a key enzyme in collagen synthesis composed of two identical alpha subunits and two beta subunits. The encoded protein is one of several different types of alpha subunits and provides the major part of the catalytic site of the active enzyme. In collagen and related proteins prolyl 4 hydroxylase catalyzes the formation of 4 hydroxyproline that is essential to the proper three dimensional folding of