ELK5069-48T, Human EDN2(Endothelin 2) ELISA Kit, 48T

ELK5069-48T, Human EDN2(Endothelin 2) ELISA Kit, 48T

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ELK5069-96T, Human EDN2(Endothelin 2) ELISA Kit, 96T

2.963,10 RON

Human EDN2(Endothelin 2) ELISA Kit

SKU
ELK5069-96T

Alternative Names: ET2; PPET2; Preproendothelin-2

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 4.66 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Cardiovascular biology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human EDN2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EDN2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 EDN2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ET2; PPET2; Preproendothelin-2

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 4.66 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Cardiovascular biology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human EDN2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EDN2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 EDN2 in the samples is then determined by comparing the OD of the samples to the standard curve.