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ELK1917-96T, Human NAGase(N-Acetyl Beta-D-Glucosaminidase) ELISA Kit, 96T

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ELK1917-48T, Human NAGase(N-Acetyl Beta-D-Glucosaminidase) ELISA Kit, 48T

2.142,00 RON

Human NAGase(N-Acetyl Beta-D-Glucosaminidase) ELISA Kit

SKU
ELK1917-48T

Alternative Names: MGEA5; MEA5; NCOAT; Hexosaminidase C; N-Acetylhexosaminidase; Hyaluronidase; Meningioma-Expressed Antigen 5; Nuclear Cytoplasmic O-GlcNAcase And Acetyltransferase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.54 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Urine

Assay length: 3.5h

Research Area: Enzyme & Kinase;Kidney biomarker;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human NAGase. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NAGase. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human NAGase, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human NAGase in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: MGEA5; MEA5; NCOAT; Hexosaminidase C; N-Acetylhexosaminidase; Hyaluronidase; Meningioma-Expressed Antigen 5; Nuclear Cytoplasmic O-GlcNAcase And Acetyltransferase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.54 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Urine

Assay length: 3.5h

Research Area: Enzyme & Kinase;Kidney biomarker;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human NAGase. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NAGase. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human NAGase, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human NAGase in the samples is then determined by comparing the OD of the samples to the standard curve.