ELK8169-96T, TG(Triglyceride) ELISA Kit, 96T

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ELK8170-96T, PGH2(Prostaglandin H2) ELISA Kit, 96T

ELK8170-96T, PGH2(Prostaglandin H2) ELISA Kit, 96T

ELK8170-48T, PGH2(Prostaglandin H2) ELISA Kit, 48T

1.814,75 RON

PGH2(Prostaglandin H2) ELISA Kit

SKU
ELK8170-48T

Alternative Names: PG-H2

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.97 pg/mL

Standard: 200 pg/mL

Detection range: 3.13-200 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Infection immunity;Endocrinology;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 PGH2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PGH2. 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 PGH2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PG-H2

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.97 pg/mL

Standard: 200 pg/mL

Detection range: 3.13-200 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Infection immunity;Endocrinology;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 PGH2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PGH2. 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 PGH2 in the samples is then determined by comparing the OD of the samples to the standard curve.