ELK9730-96T, Rat QA(Quinolinic Acid) ELISA Kit, 96T

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ELK9731-96T, Dog GHRL(Ghrelin) ELISA Kit, 96T

ELK9731-96T, Dog GHRL(Ghrelin) ELISA Kit, 96T

ELK9731-48T, Dog GHRL(Ghrelin) ELISA Kit, 48T

2.689,40 RON

Dog GHRL(Ghrelin) ELISA Kit

SKU
ELK9731-48T

Alternative Names: MTLRP; Growth Hormone-Releasing Peptide

Species: Dog

Assay Type: Competitive Inhibition

Sensitivity: 51.3 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

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

Assay length: 2h

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

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Description

Alternative Names: MTLRP; Growth Hormone-Releasing Peptide

Species: Dog

Assay Type: Competitive Inhibition

Sensitivity: 51.3 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

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

Assay length: 2h

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