ELK3981-48T, Human OAS2(2',5'-Oligoadenylate Synthetase 2) ELISA Kit, 48T

ELK3981-48T, Human OAS2(2',5'-Oligoadenylate Synthetase 2) ELISA Kit, 48T

ELK3982-48T, Human OAS3(2',5'-Oligoadenylate Synthetase 3) ELISA Kit, 48T

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ELK3981-96T, Human OAS2(2',5'-Oligoadenylate Synthetase 2) ELISA Kit, 96T

2.963,10 RON

Human OAS2(2',5'-Oligoadenylate Synthetase 2) ELISA Kit

SKU
ELK3981-96T

Alternative Names: p69 OAS / p71 OAS

Species: Human

Assay Type: Sandwich

Sensitivity: 0.3 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 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 OAS2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human OAS2. 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 OAS2, 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 OAS2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: p69 OAS / p71 OAS

Species: Human

Assay Type: Sandwich

Sensitivity: 0.3 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 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 OAS2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human OAS2. 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 OAS2, 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 OAS2 in the samples is then determined by comparing the OD of the samples to the standard curve.