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

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ELK1070-48T, Human a2M(Alpha-2-Macroglobulin) ELISA Kit, 48T

1.814,75 RON

Human a2M(Alpha-2-Macroglobulin) ELISA Kit

SKU
ELK1070-48T

Alternative Names: α2MG; α2Mg; CPAMD5; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 5

Species: Human

Assay Type: Sandwich

Sensitivity: 0.35 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: serum, plasma, urine and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;Infection immunity;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 a2M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human a2M. 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 a2M, 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 a2M in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: α2MG; α2Mg; CPAMD5; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 5

Species: Human

Assay Type: Sandwich

Sensitivity: 0.35 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: serum, plasma, urine and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;Infection immunity;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 a2M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human a2M. 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 a2M, 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 a2M in the samples is then determined by comparing the OD of the samples to the standard curve.