Descrizione Azione
Codice: 610 Confezionamento: B - 5mL (100 tests)
Dettagli
Codice: 610 Confezionamento: B - 5mL (100 tests)
Dettagli
Codice: 610 Confezionamento: A - 1mL (20 tests)
Dettagli
Codice: 610 Confezionamento: C - 7mL (2) (280 tests)
Dettagli
Codice: 610 Confezionamento: A - 1mL (20 tests)
Dettagli
Codice: CM-0951125mL×4 Confezionamento: 125mL×4
Dettagli
Codice: CM-0279125mL×4 Confezionamento: 125mL×4
Dettagli

UMOD Antibody detects endogenous levels of total UMOD.

Codice: DF6692 Confezionamento: 100ul
Dettagli

UMOD Antibody detects endogenous levels of total UMOD.

Codice: DF6692 Confezionamento: 200ul
Dettagli

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.

Codice: D-AB-10364L_100μL Confezionamento: 100μL
Dettagli

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.

Codice: D-AB-10364L_25μL Confezionamento: 25μL
Dettagli

UMP/CMP kinase Antibody detects endogenous levels of total UMP/CMP kinase.

Codice: AF9222 Confezionamento: 100ul
Dettagli