ELK9578-48T, GnRH(GonadotropinReleasing Hormone) ELISA Kit, 48T

ELK9578-48T, GnRH(GonadotropinReleasing Hormone) ELISA Kit, 48T

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ELK9578-96T, GnRH(GonadotropinReleasing Hormone) ELISA Kit, 96T

2.963,10 RON

GnRH(GonadotropinReleasing Hormone) ELISA Kit

SKU
ELK9578-96T

Alternative Names: GNRH1; GRH; HH12; LHRH; LNRH; Luliberin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 9.38 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Enzyme & Kinase;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with GnRH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to GnRH. 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 GnRH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Price 2.490,00 RON (preturile sunt fara TVA)
Description

Alternative Names: GNRH1; GRH; HH12; LHRH; LNRH; Luliberin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 9.38 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Enzyme & Kinase;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with GnRH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to GnRH. 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 GnRH in the samples is then determined by comparing the OD of the samples to the standard curve.