ELK1890-48T, AGE(Advanced Glycation End Product) ELISA Kit, 48T

ELK1890-48T, AGE(Advanced Glycation End Product) ELISA Kit, 48T

ELK1891-48T, Human AhR(Aryl Hydrocarbon Receptor) ELISA Kit, 48T

ELK1891-48T, Human AhR(Aryl Hydrocarbon Receptor) ELISA Kit, 48T

ELK1890-96T, AGE(Advanced Glycation End Product) ELISA Kit, 96T

2.475,20 RON

AGE(Advanced Glycation End Product) ELISA Kit

SKU
ELK1890-96T

Alternative Names: AGEs; Advanced Glycation End Products

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 38.2 ng/mL

Standard: 8000 ng/mL

Detection range: 125-8000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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

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Description

Alternative Names: AGEs; Advanced Glycation End Products

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 38.2 ng/mL

Standard: 8000 ng/mL

Detection range: 125-8000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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