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ELK4334-96T, Rat VDR(Vitamin D Receptor) ELISA Kit, 96T

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ELK4334-48T, Rat VDR(Vitamin D Receptor) ELISA Kit, 48T

2.142,00 RON

Rat VDR(Vitamin D Receptor) ELISA Kit

SKU
ELK4334-48T

Alternative Names: NR1I1; Nuclear Receptor Subfamily 1 Group I Member 1; Calcitriol Receptor; 1,25-dihydroxyvitamin D3 receptor

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.244 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;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 VDR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat VDR. 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 VDR, 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 VDR in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: NR1I1; Nuclear Receptor Subfamily 1 Group I Member 1; Calcitriol Receptor; 1,25-dihydroxyvitamin D3 receptor

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.244 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;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 VDR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat VDR. 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 VDR, 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 VDR in the samples is then determined by comparing the OD of the samples to the standard curve.