Recombinant Human Uromodulin GST (N-Term) Protein

This product is produced by and distributed for Abnova, a company based in Taiwan.

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. [provided by RefSeq]

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.

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Publication using H00007369-Q01	Applications	Species
Serena D Souza, Wassim Obeid, Jeanine Hernandez, David Hu, Yumeng Wen, Dennis G. Moledina, Andre Albert, Anya Gregg, Andrew Wheeler, Heather Thiessen Philbrook, Chirag R. Parikh The development of lateral flow devices for urinary biomarkers to assess kidney health Scientific Reports 2024-04-12 [PMID: 38609491]

Array H00007369-Q01

• Uromodulin Antibodies
• Uromodulin ELISA Kits
• Uromodulin Lysates
• Uromodulin Proteins
• Uromodulin ELISA