Recombinant Human RET (N-GST tag)

DESCRIPTION

RET gene codes for a transmembrane tyrosine kinase which is a subunit of a multimeric complex that acts as a receptor for four structurally related molecules: GDNF, neurturin, artemin and persephin . Germline mutations of RET cause a dominantly inherited dysgenesis of the enteric nervous system known as Hirschsprung's disease. RET is constitutively activated by point mutations in hereditary medullary thyroid carcinomas (MTCs). Several single nucleotide polymorphisms of the RET gene have been described. Multiple endocrine neoplasia type 2A (MEN 2A) have been reported to be associated with two mutations of the protooncogene RET .

DETAILS

Alias: PTC, MTC1, HSCR1, MEN2A, MEN2B, RET51, CDHF12, RET-ELE1
Purity: 70% - 90%
Source: Insect cells
Gene ID: N/A
Organism: Human
Accession: NM_020630
Functions: The specific activity of RET was determined to be 67 nmol /min/mg as per activity assay protocol
Appearance: Liquid
Solubility: N/A
Formulation: 50mM Tris-HCl, pH 7.5, 150mM NaCl, 0.25mM DTT, 0.1mM PMSF, 25% glycerol.
Gene Symbol: RET
Storage Condition: Store product at –70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Shipping Condition: Dry Ice
Molecular Weight (kDa): 74