ELK7548-96T, Rat UCN2(Urocortin 2) ELISA Kit, 96T

ELK7548-96T, Rat UCN2(Urocortin 2) ELISA Kit, 96T

ELK7549-96T, Rat ADH3(Alcohol Dehydrogenase 3) ELISA Kit, 96T

ELK7549-96T, Rat ADH3(Alcohol Dehydrogenase 3) ELISA Kit, 96T

ELK7549-48T, Rat ADH3(Alcohol Dehydrogenase 3) ELISA Kit, 48T

2.142,00 RON

Rat ADH3(Alcohol Dehydrogenase 3) ELISA Kit

SKU
ELK7549-48T

Alternative Names: ADH1C; Alcohol dehydrogenase subunit gamma

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.138 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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 Rat ADH3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ADH3. 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 Rat ADH3, 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 Rat ADH3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ADH1C; Alcohol dehydrogenase subunit gamma

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.138 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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 Rat ADH3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ADH3. 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 Rat ADH3, 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 Rat ADH3 in the samples is then determined by comparing the OD of the samples to the standard curve.