ELK0479-96T, Human cPLA2(Cytosolic Phospholipase A2) ELISA Kit, 96T

ELK0479-96T, Human cPLA2(Cytosolic Phospholipase A2) ELISA Kit, 96T

ELK047ES-96T, EasyStep Rat PG(Progesterone) ELISA Kit, 96T

ELK047ES-96T, EasyStep Rat PG(Progesterone) ELISA Kit, 96T

ELK047ES-48T, EasyStep Rat PG(Progesterone) ELISA Kit, 48T

2.689,40 RON

EasyStep Rat PG(Progesterone) ELISA Kit

SKU
ELK047ES-48T

Alternative Names: P4; Pregn-4-Ene-3,20-Dione

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.7 ng/mL

Standard: 100 ng/mL

Detection range: 1.56-100 ng/mL

Sample type: Serum, plasma

Assay length: 1.5h

Research Area: Endocrinology;Reproductive science;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 PG antigen, and the Rat PG standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat PG 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 PG in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: P4; Pregn-4-Ene-3,20-Dione

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.7 ng/mL

Standard: 100 ng/mL

Detection range: 1.56-100 ng/mL

Sample type: Serum, plasma

Assay length: 1.5h

Research Area: Endocrinology;Reproductive science;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 PG antigen, and the Rat PG standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat PG 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 PG in the samples is then determined by comparing the OD of the samples to the standard curve.