ELK045ES-48T, EasyStep Human PG(Progesterone) ELISA Kit, 48T

ELK045ES-48T, EasyStep Human PG(Progesterone) ELISA Kit, 48T

ELK0460-48T, Human FATP3(Fatty Acid Transport Protein 3) ELISA Kit, 48T

ELK0460-48T, Human FATP3(Fatty Acid Transport Protein 3) ELISA Kit, 48T

ELK045ES-96T, EasyStep Human PG(Progesterone) ELISA Kit, 96T

3.736,60 RON

EasyStep Human PG(Progesterone) ELISA Kit

SKU
ELK045ES-96T

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

Species: Human

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 Human PG antigen, and the Human 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 Human 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 Human 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: Human

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 Human PG antigen, and the Human 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 Human 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 Human PG in the samples is then determined by comparing the OD of the samples to the standard curve.