ELK1070-96T, Human a2M(Alpha-2-Macroglobulin) ELISA Kit, 96T

ELK1070-96T, Human a2M(Alpha-2-Macroglobulin) ELISA Kit, 96T

ELK1071-96T, Human ALB(Albumin) ELISA Kit, 96T

ELK1071-96T, Human ALB(Albumin) ELISA Kit, 96T

ELK1071-48T, Human ALB(Albumin) ELISA Kit, 48T

1.814,75 RON

Human ALB(Albumin) ELISA Kit

SKU
ELK1071-48T

Alternative Names: Serum albumin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 89.6 ng/mL

Standard: 20000 ng/mL

Detection range: 312.5-20000 ng/mL

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

Assay length: 2h

Research Area: Tumor immunity;Infection immunity;Hematology;Hepatology;Nutrition metabolism;

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

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Description

Alternative Names: Serum albumin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 89.6 ng/mL

Standard: 20000 ng/mL

Detection range: 312.5-20000 ng/mL

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

Assay length: 2h

Research Area: Tumor immunity;Infection immunity;Hematology;Hepatology;Nutrition metabolism;

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