ELK2242-96T, Mouse LDH(Lactate Dehydrogenase) ELISA Kit, 96T

ELK2242-96T, Mouse LDH(Lactate Dehydrogenase) ELISA Kit, 96T

ELK2243-96T, Human AP36(Apelin 36) ELISA Kit, 96T

ELK2243-96T, Human AP36(Apelin 36) ELISA Kit, 96T

ELK2243-48T, Human AP36(Apelin 36) ELISA Kit, 48T

2.142,00 RON

Human AP36(Apelin 36) ELISA Kit

SKU
ELK2243-48T

Alternative Names: APLN36

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 2.52 pg/mL

Standard: 600 pg/mL

Detection range: 9.38-600 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Gastroenterology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human AP36 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP36. 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 Human AP36 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: APLN36

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 2.52 pg/mL

Standard: 600 pg/mL

Detection range: 9.38-600 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Gastroenterology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human AP36 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP36. 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 Human AP36 in the samples is then determined by comparing the OD of the samples to the standard curve.