NDRG1 Polyclonal Antibody, 100ul Metabolic enzymes An allele mutation and a

An allele mutation and a low-frequency noncoding single-nucleotide polymorphism (SNP) in this gene cause thrombocytopenia-absent radius (TAR) syndrome

The encoded receptor undergoes fast agonist-induced internalization through clathrin-coated pits and is subsequently recycled back to the cell membrane

4-galactosyltransferase 3) encodes an enzyme that may be mainly involved in the synthesis of the first N-acetyllactosamine unit of poly-N-acetyllactosamine chains

KCNA1 encodes a voltage-gated delayed potassium channel that is phylogenetically related to the Drosophila Shaker channel

NDRG1 Polyclonal Antibody, 100ul Metabolic enzymes An allele mutation and aThis gene is a member of the N myc downregulated gene family which belongs to the alpha beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. The encoded protein is necessary for p53 mediated caspase activation and apoptosis. Mutations in this gene are a cause of Charcot Marie Tooth disease type 4D, and expression of this gene may be a