PGE2(Prostaglandin E2) ELISA Kit

Reactivity: General
Assay range: 2.47-200pg/mL
Sensitivity: < 0.84pg/mL
Detection Method: Competitive Inhibition
Size: 48T, 96T
Storage: 2-8 ℃ for 6 months
CV (%): Intra-Assay: CV<8%; Inter-Assay: CV<10%

PGE2(Prostaglandin E2) Basic information

Prostaglandin E2 (PGE2), also known as dinoprostone, is a naturally occurring prostaglandin with oxytocic properties that is used as a medication. Dinoprostone is used in labor induction, bleeding after delivery, termination of pregnancy, and in newborn babies to keep the ductus arteriosus open. In babies it is used in those with congenital heart defects until surgery can be carried out. It is also used to manage gestational trophoblastic disease. It may be used within the vagina or by injection into a vein. PGE2 synthesis within the body begins with the activation of arachidonic acid (AA) by the enzyme phospholipase A2. Once activated, AA is oxygenated by cyclooxygenase (COX) enzymes to form prostaglandin endoperoxides. Specifically, prostaglandin G2 (PGG2) is modified by the peroxidase moiety of the COX enzyme to produce prostaglandin H2 (PGH2) which is then converted to PGE2.

PGE2(Prostaglandin E2) ELISA Kit test method

Feiyue’s PGE2(Prostaglandin E2) is an ELISA reagent for detection of PGE2(Prostaglandin E2) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.

This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with target. During the reaction, target in the sample or standard competes with a fixed amount of target on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to target. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm. The concentration of target in the samples is then determined by comparing the OD of the samples to the standard curve. 

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Контактное лицо: Agnes