ELK3033-48T, Human ETRA(Endothelin Receptor A) ELISA Kit, 48T

ELK3033-48T, Human ETRA(Endothelin Receptor A) ELISA Kit, 48T

ELK3034-48T, Human PAPPA2(Pappalysin 2) ELISA Kit, 48T

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ELK3033-96T, Human ETRA(Endothelin Receptor A) ELISA Kit, 96T

2.963,10 RON

Human ETRA(Endothelin Receptor A) ELISA Kit

SKU
ELK3033-96T

Alternative Names: EDNRA; ETA; ETR-A; Endothelin A receptor; Endothelin-1 receptor

Species: Human

Assay Type: Sandwich

Sensitivity: 0.115 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

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

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Description

Alternative Names: EDNRA; ETA; ETR-A; Endothelin A receptor; Endothelin-1 receptor

Species: Human

Assay Type: Sandwich

Sensitivity: 0.115 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

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