ELK8072-48T, PAF(Platelet Activating Factor) ELISA Kit, 48T

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ELK8072-96T, PAF(Platelet Activating Factor) ELISA Kit, 96T

2.475,20 RON

PAF(Platelet Activating Factor) ELISA Kit

SKU
ELK8072-96T

Alternative Names: PAF-Acether; AGEPC; Acetyl-Glyceryl-Ether-Phosphorylcholine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 14.4 pg/mL

Standard: 3000 pg/mL

Detection range: 46.88-3000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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

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Description

Alternative Names: PAF-Acether; AGEPC; Acetyl-Glyceryl-Ether-Phosphorylcholine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 14.4 pg/mL

Standard: 3000 pg/mL

Detection range: 46.88-3000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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