Human Uromucoid (UMOD) ELISA KIT (1 x 96 wells)

CAT#: EA102492

For quantitative detection of human Uromodulin in cell culture supernates, serum and plasma (heparin).



CNY 5330.00


货期*
3周

规格
    • 1 x 96 wells

Product images

Specifications

Product Data
Description For quantitative detection of human Uromodulin in cell culture supernates, serum and plasma (heparin).
Size 1 x 96 wells
Format 8x12 divisible strips
Assay Type Sandwich ELISA kit of Quantitative Detection for Human UMOD
Assay Length 3.5 hours incubations; 1 hour washing and analyzing samples
Signal Colorimetric
Curve Range 312pg/ml-20000pg/ml
Specificity This kit is used for quantitative detection of Human UMOD
Sensitivity <10pg/ml
Reactivity Human
Cross Reactivity There is no detectable cross-reactivity with other relevant proteins.
Components
  • 96-well plate precoated with anti- human Uromodulin antibody | 1
  • Lyophilized recombinant human Uromodulin standard | 10ng/tubex2 | 1
  • Biotinylated anti- human Uromodulin antibody 100 ul | 1
  • Avidin-Biotin-Peroxidase Complex(ABC) 100 ul | 1
  • Sample diluent buffer 30 ml | 1
  • Antibody diluent buffer 12 ml | 1
  • ABC diluent buffer 12 ml | 1
  • TMB color developing agent 10ml | 1
  • TMB stop solution 10 ml | 1
  • Wash Buffer (25x) 20 ml | 1
  • Plate Sealers | 4
Background The Tamm–Horsfall glycoprotein (THP), also known as uromodulin, is a glycoprotein that in humans is encoded by the UMOD gene. The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. 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. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants.
Gene Symbol UMOD
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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