ELK5186-96T, Human BK(Bradykinin) ELISA Kit, 96T

ELK5186-96T, Human BK(Bradykinin) ELISA Kit, 96T

ELK5187-96T, Human EM2(Endomorphin 2) ELISA Kit, 96T

ELK5187-96T, Human EM2(Endomorphin 2) ELISA Kit, 96T

ELK5187-48T, Human EM2(Endomorphin 2) ELISA Kit, 48T

2.142,00 RON

Human EM2(Endomorphin 2) ELISA Kit

SKU
ELK5187-48T

Alternative Names: EP2

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 1.56 pg/mL

Standard: 300 pg/mL

Detection range: 4.69-300 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Neuro science;Gastroenterology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human EM2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EM2. 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 EM2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: EP2

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 1.56 pg/mL

Standard: 300 pg/mL

Detection range: 4.69-300 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Neuro science;Gastroenterology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human EM2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EM2. 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 EM2 in the samples is then determined by comparing the OD of the samples to the standard curve.