ELK6761-48T, Rat DAB1(Disabled Homolog 1) ELISA Kit, 48T

ELK6761-48T, Rat DAB1(Disabled Homolog 1) ELISA Kit, 48T

ELK6762-48T, Mouse DHODH(Dihydroorotate Dehydrogenase) ELISA Kit, 48T

ELK6762-48T, Mouse DHODH(Dihydroorotate Dehydrogenase) ELISA Kit, 48T

ELK6761-96T, Rat DAB1(Disabled Homolog 1) ELISA Kit, 96T

2.963,10 RON

Rat DAB1(Disabled Homolog 1) ELISA Kit

SKU
ELK6761-96T

Alternative Names: Dab 1; Dab reelin signal transducer 1; Dab

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.107 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;

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 Rat DAB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat DAB1. 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 Rat DAB1, 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 Rat DAB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Dab 1; Dab reelin signal transducer 1; Dab

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.107 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;

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 Rat DAB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat DAB1. 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 Rat DAB1, 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 Rat DAB1 in the samples is then determined by comparing the OD of the samples to the standard curve.