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Recombinant Human UMOD cell lysate

Cat.No.: UMOD-1885HCL
Description: This gene encodes uromodulin, the most abundant protein in normal urine. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. Uromodulin may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of uromodulin in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the autosomal dominant renal disorders medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: UMOD uromodulin [ Homo sapiens ]
Official Symbol: UMOD
Synonyms: UMOD; uromodulin; uromodulin (uromucoid, Tamm Horsfall glycoprotein); Tamm Horsfall glycoprotein; uromucoid; Tamm-Horsfall glycoprotein; tamm-Horsfall urinary glycoprotein; uromodulin (uromucoid, Tamm-Horsfall glycoprotein); THP; FJHN; HNFJ; THGP; HNFJ1; MCKD2; ADMCKD2;
Gene ID: 7369
mRNA Refseq: NM_001008389
Protein Refseq: NP_001008390
MIM: 191845
UniProt ID: P07911
Chromosome Location: 16p12.3
Function: calcium ion binding;

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