ELK4988-48T, Human XRCC2(X-Ray Repair Cross Complementing 2) ELISA Kit, 48T

ELK4988-48T, Human XRCC2(X-Ray Repair Cross Complementing 2) ELISA Kit, 48T

ELK4989-48T, H2A(Histone H2A) ELISA Kit, 48T

ELK4989-48T, H2A(Histone H2A) ELISA Kit, 48T

ELK4988-96T, Human XRCC2(X-Ray Repair Cross Complementing 2) ELISA Kit, 96T

2.963,10 RON

Human XRCC2(X-Ray Repair Cross Complementing 2) ELISA Kit

SKU
ELK4988-96T

Alternative Names: DNA repair protein XRCC2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.114 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids.

Assay length: 3.5h

Research Area: Tumor immunity;

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 XRCC2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human XRCC2. 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 XRCC2, 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 XRCC2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: DNA repair protein XRCC2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.114 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids.

Assay length: 3.5h

Research Area: Tumor immunity;

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 XRCC2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human XRCC2. 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 XRCC2, 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 XRCC2 in the samples is then determined by comparing the OD of the samples to the standard curve.