ELK4069-48T, Human APLN(Apelin) ELISA Kit, 48T

ELK4069-48T, Human APLN(Apelin) ELISA Kit, 48T

ELK4070-48T, Human HBg1(Hemoglobin Gamma 1) ELISA Kit, 48T

ELK4070-48T, Human HBg1(Hemoglobin Gamma 1) ELISA Kit, 48T

ELK4069-96T, Human APLN(Apelin) ELISA Kit, 96T

2.963,10 RON

Human APLN(Apelin) ELISA Kit

SKU
ELK4069-96T

Alternative Names: XNPEP2; APEL; APJ endogenous ligand

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 8.25 pg/mL

Standard: 1600 pg/mL

Detection range: 25-1600 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Endocrinology;

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

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Description

Alternative Names: XNPEP2; APEL; APJ endogenous ligand

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 8.25 pg/mL

Standard: 1600 pg/mL

Detection range: 25-1600 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Endocrinology;

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