ELK1973-48T, Human DbH(Dopamine Beta Hydroxylase) ELISA Kit, 48T

ELK1973-48T, Human DbH(Dopamine Beta Hydroxylase) ELISA Kit, 48T

ELK1974-48T, Human TH(Tyrosine Hydroxylase) ELISA Kit, 48T

ELK1974-48T, Human TH(Tyrosine Hydroxylase) ELISA Kit, 48T

ELK1973-96T, Human DbH(Dopamine Beta Hydroxylase) ELISA Kit, 96T

2.963,10 RON

Human DbH(Dopamine Beta Hydroxylase) ELISA Kit

SKU
ELK1973-96T

Alternative Names: DBM; Dopamine Beta-Monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 1.31 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Neuro science;

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

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Description

Alternative Names: DBM; Dopamine Beta-Monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 1.31 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Neuro science;

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