ELK6914-48T, Rat ADRb2(Adrenergic Receptor Beta 2) ELISA Kit, 48T

ELK6914-48T, Rat ADRb2(Adrenergic Receptor Beta 2) ELISA Kit, 48T

ELK6915-48T, Rat ADRb3(Adrenergic Receptor Beta 3) ELISA Kit, 48T

ELK6915-48T, Rat ADRb3(Adrenergic Receptor Beta 3) ELISA Kit, 48T

ELK6914-96T, Rat ADRb2(Adrenergic Receptor Beta 2) ELISA Kit, 96T

2.963,10 RON

Rat ADRb2(Adrenergic Receptor Beta 2) ELISA Kit

SKU
ELK6914-96T

Alternative Names: B2AR; Beta-2 adrenoreceptor

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.058 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Endocrinology;

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 ADRb2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ADRb2. 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 ADRb2, 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 ADRb2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: B2AR; Beta-2 adrenoreceptor

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.058 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Endocrinology;

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 ADRb2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ADRb2. 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 ADRb2, 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 ADRb2 in the samples is then determined by comparing the OD of the samples to the standard curve.