ELK4514-96T, Human HSP-70/HSPA9(HeatShock Protein 70) ELISA Kit, 96T

ELK4514-96T, Human HSP-70/HSPA9(HeatShock Protein 70) ELISA Kit, 96T

ELK4515-96T, Human ADH2(Alcohol Dehydrogenase 2) ELISA Kit, 96T

ELK4515-96T, Human ADH2(Alcohol Dehydrogenase 2) ELISA Kit, 96T

ELK4515-48T, Human ADH2(Alcohol Dehydrogenase 2) ELISA Kit, 48T

2.142,00 RON

Human ADH2(Alcohol Dehydrogenase 2) ELISA Kit

SKU
ELK4515-48T

Alternative Names: ADH1B; Alcohol dehydrogenase subunit beta

Species: Human

Assay Type: Sandwich

Sensitivity: 12.9 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/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 Human ADH2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ADH2. 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 ADH2, 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 ADH2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ADH1B; Alcohol dehydrogenase subunit beta

Species: Human

Assay Type: Sandwich

Sensitivity: 12.9 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/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 Human ADH2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ADH2. 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 ADH2, 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 ADH2 in the samples is then determined by comparing the OD of the samples to the standard curve.