ELK8709-96T, Goat MDA(Malondialdehyde) ELISA Kit, 96T

ELK8709-96T, Goat MDA(Malondialdehyde) ELISA Kit, 96T

ELK8711-96T, Rat PGE2(Prostaglandin E2) ELISA Kit, 96T

ELK8711-96T, Rat PGE2(Prostaglandin E2) ELISA Kit, 96T

ELK8711-48T, Rat PGE2(Prostaglandin E2) ELISA Kit, 48T

1.814,75 RON

Rat PGE2(Prostaglandin E2) ELISA Kit

SKU
ELK8711-48T

Alternative Names: PG-E2

Species: Rat

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 Rat PGE2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat PGE2. 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 Rat PGE2 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-E2

Species: Rat

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 Rat PGE2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat PGE2. 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 Rat PGE2 in the samples is then determined by comparing the OD of the samples to the standard curve.