ELK3799-96T, Human RS(Retinoschisin) ELISA Kit, 96T

ELK3799-96T, Human RS(Retinoschisin) ELISA Kit, 96T

ELK3800-96T, Human CH25H(Cholesterol-25-Hydroxylase) ELISA Kit, 96T

ELK3800-96T, Human CH25H(Cholesterol-25-Hydroxylase) ELISA Kit, 96T

ELK3800-48T, Human CH25H(Cholesterol-25-Hydroxylase) ELISA Kit, 48T

2.142,00 RON

Human CH25H(Cholesterol-25-Hydroxylase) ELISA Kit

SKU
ELK3800-48T

Alternative Names: h25OH; Cholesterol 25-monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 49 pg/mL

Standard: 8000 pg/mL

Detection range: 125-8000 pg/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 CH25H. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CH25H. 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 CH25H, 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 CH25H in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: h25OH; Cholesterol 25-monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 49 pg/mL

Standard: 8000 pg/mL

Detection range: 125-8000 pg/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 CH25H. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CH25H. 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 CH25H, 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 CH25H in the samples is then determined by comparing the OD of the samples to the standard curve.