ELK9891-48T, Human αHBDH(Alpha Hydroxybutyrate Dehydrogenase) ELISA Kit, 48T

ELK9891-48T, Human αHBDH(Alpha Hydroxybutyrate Dehydrogenase) ELISA Kit, 48T

ELK9892-48T, Human FXN(Frataxin) ELISA Kit, 48T

ELK9892-48T, Human FXN(Frataxin) ELISA Kit, 48T

ELK9891-96T, Human αHBDH(Alpha Hydroxybutyrate Dehydrogenase) ELISA Kit, 96T

2.963,10 RON

Human αHBDH(Alpha Hydroxybutyrate Dehydrogenase) ELISA Kit

SKU
ELK9891-96T

Alternative Names: α-hydroxybutyrate dehydrogenase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.055 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 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 αHBDH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human αHBDH. 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 αHBDH, 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 αHBDH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: α-hydroxybutyrate dehydrogenase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.055 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 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 αHBDH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human αHBDH. 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 αHBDH, 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 αHBDH in the samples is then determined by comparing the OD of the samples to the standard curve.