ELK8874-48T, Rat a1BG(Alpha-1-B-Glycoprotein) ELISA Kit, 48T

ELK8874-48T, Rat a1BG(Alpha-1-B-Glycoprotein) ELISA Kit, 48T

ELK8875-48T, Sheep SPB(Surfactant Associated Protein B) ELISA Kit, 48T

ELK8875-48T, Sheep SPB(Surfactant Associated Protein B) ELISA Kit, 48T

ELK8874-96T, Rat a1BG(Alpha-1-B-Glycoprotein) ELISA Kit, 96T

2.963,10 RON

Rat a1BG(Alpha-1-B-Glycoprotein) ELISA Kit

SKU
ELK8874-96T

Alternative Names: Alpha 1 B Glycoprotein; Alpha 1 beta Glycoprotein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.147 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Immune molecule;

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 a1BG. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat a1BG. 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 a1BG, 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 a1BG in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Alpha 1 B Glycoprotein; Alpha 1 beta Glycoprotein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.147 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Immune molecule;

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 a1BG. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat a1BG. 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 a1BG, 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 a1BG in the samples is then determined by comparing the OD of the samples to the standard curve.