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ELK8558-48T, Human GSP(Glycated Serum Protein) ELISA Kit, 48T

2.142,00 RON

Human GSP(Glycated Serum Protein) ELISA Kit

SKU
ELK8558-48T

Alternative Names: GSP

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 10.19 nmol/mL

Standard: 2000 nmol/mL

Detection range: 31.25-2000 nmol/mL

Sample type: serum, plasma

Assay length: 2h

Research Area: Diabetes

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

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Description

Alternative Names: GSP

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 10.19 nmol/mL

Standard: 2000 nmol/mL

Detection range: 31.25-2000 nmol/mL

Sample type: serum, plasma

Assay length: 2h

Research Area: Diabetes

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