ELK7266-96T, Rat XBP1(X-Box Binding Protein 1) ELISA Kit, 96T

ELK7266-96T, Rat XBP1(X-Box Binding Protein 1) ELISA Kit, 96T

ELK7267-96T, Rat GLRa2(Glycine Receptor Alpha 2) ELISA Kit, 96T

ELK7267-96T, Rat GLRa2(Glycine Receptor Alpha 2) ELISA Kit, 96T

ELK7267-48T, Rat GLRa2(Glycine Receptor Alpha 2) ELISA Kit, 48T

2.142,00 RON

Rat GLRa2(Glycine Receptor Alpha 2) ELISA Kit

SKU
ELK7267-48T

Alternative Names: GLR

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.115 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: tissue homogenates, cell lysates 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 Rat GLRa2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GLRa2. 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 GLRa2, 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 GLRa2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: GLR

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.115 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: tissue homogenates, cell lysates 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 Rat GLRa2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GLRa2. 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 GLRa2, 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 GLRa2 in the samples is then determined by comparing the OD of the samples to the standard curve.