ELK8685-48T, Rat ARRb1(Arrestin Beta 1) ELISA Kit, 48T

ELK8685-48T, Rat ARRb1(Arrestin Beta 1) ELISA Kit, 48T

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ELK8685-96T, Rat ARRb1(Arrestin Beta 1) ELISA Kit, 96T

2.963,10 RON

Rat ARRb1(Arrestin Beta 1) ELISA Kit

SKU
ELK8685-96T

Alternative Names: ARB1; ARR1; ARR-B1; Arrestin 2; Beta Arrestin-1

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.053 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: Signal transduction;Endocrinology;Neuro science;Hormone metabolism;

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 ARRb1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ARRb1. 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 ARRb1, 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 ARRb1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ARB1; ARR1; ARR-B1; Arrestin 2; Beta Arrestin-1

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.053 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: Signal transduction;Endocrinology;Neuro science;Hormone metabolism;

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 ARRb1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ARRb1. 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 ARRb1, 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 ARRb1 in the samples is then determined by comparing the OD of the samples to the standard curve.