ELK8960-48T, Horse IgA(Immunoglobulin A) ELISA Kit, 48T

ELK8960-48T, Horse IgA(Immunoglobulin A) ELISA Kit, 48T

ELK8961-48T, Horse CP(Ceruloplasmin) ELISA Kit, 48T

ELK8961-48T, Horse CP(Ceruloplasmin) ELISA Kit, 48T

ELK8960-96T, Horse IgA(Immunoglobulin A) ELISA Kit, 96T

3.736,60 RON

Horse IgA(Immunoglobulin A) ELISA Kit

SKU
ELK8960-96T

Alternative Names: Immunoglobulin A

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.34 µg/mL

Standard: 50 µg/mL

Detection range: 0.79-50 µg/mL

Sample type: Serum, plasma, saliva and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;Immune molecule;Hematology;Pulmonology;

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 Horse IgA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse IgA. 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 Horse IgA, 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 Horse IgA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Immunoglobulin A

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.34 µg/mL

Standard: 50 µg/mL

Detection range: 0.79-50 µg/mL

Sample type: Serum, plasma, saliva and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;Immune molecule;Hematology;Pulmonology;

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 Horse IgA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse IgA. 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 Horse IgA, 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 Horse IgA in the samples is then determined by comparing the OD of the samples to the standard curve.