ELK4961-96T, Rat FABP6(Fatty Acid Binding Protein 6, Ileal) ELISA Kit, 96T

ELK4961-96T, Rat FABP6(Fatty Acid Binding Protein 6, Ileal) ELISA Kit, 96T

ELK4962-96T, Human HBg2(Hemoglobin Gamma 2) ELISA Kit, 96T

ELK4962-96T, Human HBg2(Hemoglobin Gamma 2) ELISA Kit, 96T

ELK4962-48T, Human HBg2(Hemoglobin Gamma 2) ELISA Kit, 48T

2.142,00 RON

Human HBg2(Hemoglobin Gamma 2) ELISA Kit

SKU
ELK4962-48T

Alternative Names: Gamma-2-globin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.62 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

Sample type: Serum, plasma, erythrocyte lysates.

Assay length: 3.5h

Research Area: Hematology;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human HBg2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HBg2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human HBg2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 HBg2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Gamma-2-globin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.62 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

Sample type: Serum, plasma, erythrocyte lysates.

Assay length: 3.5h

Research Area: Hematology;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human HBg2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HBg2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human HBg2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 HBg2 in the samples is then determined by comparing the OD of the samples to the standard curve.