ELK4142-48T, Human NAT1(N-Acetyltransferase 1) ELISA Kit, 48T

ELK4142-48T, Human NAT1(N-Acetyltransferase 1) ELISA Kit, 48T

ELK4143-48T, Human EXT1(Exostoses 1) ELISA Kit, 48T

ELK4143-48T, Human EXT1(Exostoses 1) ELISA Kit, 48T

ELK4142-96T, Human NAT1(N-Acetyltransferase 1) ELISA Kit, 96T

2.963,10 RON

Human NAT1(N-Acetyltransferase 1) ELISA Kit

SKU
ELK4142-96T

Alternative Names: AAC1; Arylamine N-Acetyltransferase; Arylamide acetylase 1; Monomorphic arylamine N-acetyltransferase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.61 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Enzyme & Kinase;

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 NAT1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NAT1. 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 NAT1, 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 NAT1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: AAC1; Arylamine N-Acetyltransferase; Arylamide acetylase 1; Monomorphic arylamine N-acetyltransferase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.61 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Enzyme & Kinase;

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 NAT1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NAT1. 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 NAT1, 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 NAT1 in the samples is then determined by comparing the OD of the samples to the standard curve.