Anticorps relatifs à l’épigénétique

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 Mouse Cit H3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse Cit H3. 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 Mouse Cit H3, 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 Mouse Cit H3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 STAB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human STAB1. 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 STAB1, 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 STAB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 SALL4. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SALL4. 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 SALL4, 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 SALL4 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 ATXN2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ATXN2. 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 ATXN2, 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 ATXN2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Mouse SREBP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse SREBP2. 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 Mouse SREBP2, 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 Mouse SREBP2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Mouse Cit H3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse Cit H3. 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 Mouse Cit H3, 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 Mouse Cit H3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 KDM2B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human KDM2B. 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 KDM2B, 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 KDM2B in the samples is then determined by comparing the OD of the samples to the standard curve.

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 MSH6. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MSH6. 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 MSH6, 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 MSH6 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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

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 STAB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human STAB1. 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 STAB1, 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 STAB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 SOX17. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SOX17. 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 SOX17, 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 SOX17 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 LONP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LONP1. 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 LONP1, 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 LONP1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 ZEB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ZEB1. 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 ZEB1, 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 ZEB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Rabbit SREBP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit SREBP1. 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 Rabbit SREBP1, 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 Rabbit SREBP1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Rat Cit H3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat Cit H3. 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 Rat Cit H3, 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 Rat Cit H3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 NRF1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NRF1. 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 NRF1, 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 NRF1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 IFI16. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IFI16. 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 IFI16, 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 IFI16 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Rat SREBP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat SREBP2. 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 Rat SREBP2, 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 Rat SREBP2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 ERCC3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ERCC3. 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 ERCC3, 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 ERCC3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 ATXN2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ATXN2. 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 ATXN2, 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 ATXN2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 SAM68. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SAM68. 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 SAM68, 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 SAM68 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 RAD51B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RAD51B. 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 RAD51B, 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 RAD51B in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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

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

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 Acetyl-H3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Acetyl-H3. 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 Acetyl-H3, 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 Acetyl-H3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 RPL13. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RPL13. 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 RPL13, 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 RPL13 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 NFE2L3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NFE2L3. 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 NFE2L3, 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 NFE2L3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Mouse SREBP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse SREBP1. 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 Mouse SREBP1, 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 Mouse SREBP1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 P4HTM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human P4HTM. 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 P4HTM, 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 P4HTM in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 ABL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ABL1. 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 ABL1, 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 ABL1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 FOXC2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human FOXC2. 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 FOXC2, 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 FOXC2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Cit H3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Cit H3. 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 Cit H3, 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 Cit H3 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 SALL4. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SALL4. 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 SALL4, 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 SALL4 in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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 Rat SREBP-1C. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat SREBP-1C. 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 Rat SREBP-1C, 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 Rat SREBP-1C in the samples is then determined by comparing the OD of the samples to the standard curve.

Anti-Mono-methyl-Histone H3.1 (Arg17) Antibody (8Q535) is an antibody targeting Mono-methyl-Histone H3.1 (Arg17). Anti-Mono-methyl-Histone H3.1 (Arg17) Antibody (8Q535) can be used in ELISA, WB, ICC, IF.

Anti-NKX2-1 Antibody (6Z966) is an antibody targeting NKX2-1. Anti-NKX2-1 Antibody (6Z966) can be used in ELISA, WB, IHC, FCM.

Anti-Phospho-ATM (Ser1981) Antibody (3I272) is an antibody targeting Phospho-ATM (Ser1981). Anti-Phospho-ATM (Ser1981) Antibody (3I272) can be used in ELISA, IF.

Anti-Phospho-MYC (Thr58, Ser62) Antibody (8I87) is an antibody targeting Phospho-MYC (Thr58, Ser62). Anti-Phospho-MYC (Thr58, Ser62) Antibody (8I87) can be used in ELISA, WB.

Anti-MGMT Antibody (9E151) is an antibody targeting MGMT. Anti-MGMT Antibody (9E151) can be used in ELISA, WB, IHC.

Anti-RPS19 Antibody (9B532) is an antibody targeting RPS19. Anti-RPS19 Antibody (9B532) can be used in ELISA, WB, FCM.

Anti-Phospho-MYB (Ser11) Antibody (6E104) is an antibody targeting Phospho-MYB (Ser11). Anti-Phospho-MYB (Ser11) Antibody (6E104) can be used in ELISA, IF.

Anti-Phospho-EIF2S1 (Ser51) Antibody (2L872) is an antibody targeting Phospho-EIF2S1 (Ser51). Anti-Phospho-EIF2S1 (Ser51) Antibody (2L872) can be used in ELISA, WB, IHC, IF.

Anti-SUZ12 Antibody (1Q624) is an antibody targeting SUZ12. Anti-SUZ12 Antibody (1Q624) can be used in ELISA, WB, IHC, IP.

Anti-Phospho-Histone H3.3 (Thr3) Antibody (2G840) is an antibody targeting Phospho-Histone H3.3 (Thr3). Anti-Phospho-Histone H3.3 (Thr3) Antibody (2G840) can be used in ELISA, WB, ICC, FCM.

Anti-Phospho-Histone H3.1(Ser10) Antibody (6R499) is an antibody targeting Phospho-Histone H3.1(Ser10). Anti-Phospho-Histone H3.1(Ser10) Antibody (6R499) can be used in ELISA, WB, ICC, IF.

Anti-WDR5 Antibody (8H847) is an antibody targeting WDR5. Anti-WDR5 Antibody (8H847) can be used in ELISA, IHC, FCM.

<p>Anti-HDAC9 Antibody (7A288) is an antibody targeting HDAC9. Anti-HDAC9 Antibody (7A288) can be used in ELISA, WB, IHC, IF.</p>

Anti-DGCR8 Antibody (2I601) is an antibody targeting DGCR8. Anti-DGCR8 Antibody (2I601) can be used in ELISA, WB.

Anti-EIF4A1 Antibody (5Z864) is an antibody targeting EIF4A1. Anti-EIF4A1 Antibody (5Z864) can be used in ELISA, WB, IF.

Anti-DDX5 Antibody (4I744) is an antibody targeting DDX5. Anti-DDX5 Antibody (4I744) can be used in ELISA, WB, IHC, IF, FCM.

Anti-Histone H3.3 Antibody (5V726) is an antibody targeting Histone H3.3. Anti-Histone H3.3 Antibody (5V726) can be used in ELISA, IHC, IF.

Anti-FOXO3 Antibody (7C993) is an antibody targeting FOXO3. Anti-FOXO3 Antibody (7C993) can be used in ELISA, WB, IHC, IF.

Anti-HMGB1 Antibody (7T579) is an antibody targeting HMGB1. Anti-HMGB1 Antibody (7T579) can be used in ELISA, WB, IHC.

Anti-H2AFX Antibody (1H690) is an antibody targeting H2AFX. Anti-H2AFX Antibody (1H690) can be used in ELISA, IHC, FCM.

Anti-DOT1L Antibody (6U296) is an antibody targeting DOT1L. Anti-DOT1L Antibody (6U296) can be used in ELISA, WB.

Anti-DNMT1 Antibody (2S499) is an antibody targeting DNMT1. Anti-DNMT1 Antibody (2S499) can be used in ELISA, IHC, IF.

Anti-HIST1H3A Antibody (7S938) is an antibody targeting HIST1H3A. Anti-HIST1H3A Antibody (7S938) can be used in ELISA, WB, IHC, IF.

Anti-Histone H2B type 1-K Antibody (6I202) is an antibody targeting Histone H2B type 1-K. Anti-Histone H2B type 1-K Antibody (6I202) can be used in ELISA, WB, IHC.

Anti-Histone H4 Antibody (6F126) is an antibody targeting Histone H4. Anti-Histone H4 Antibody (6F126) can be used in ELISA, IHC, FCM.

Anti-EIF5A Antibody (4P149) is an antibody targeting EIF5A. Anti-EIF5A Antibody (4P149) can be used in ELISA, WB, IHC, IF, FCM.

Anti-Di-methyl-Histone H3.1 (Lys9) Antibody (9G554) is an antibody targeting Di-methyl-Histone H3.1 (Lys9). Anti-Di-methyl-Histone H3.1 (Lys9) Antibody (9G554) can be used in ELISA, WB, IF.

Anti-DDX6 Antibody (4N492) is an antibody targeting DDX6. Anti-DDX6 Antibody (4N492) can be used in ELISA, IHC.

Anti-FOXA1 Antibody (9G114) is an antibody targeting FOXA1. Anti-FOXA1 Antibody (9G114) can be used in ELISA, WB, IHC, IP.

Anti-KIFAP3 Antibody (2F836) is an antibody targeting KIFAP3. Anti-KIFAP3 Antibody (2F836) can be used in ELISA, WB, IHC, IF.

Anti-Formyl-HIST1H3A (K122) Antibody (5T153) is an antibody targeting Formyl-HIST1H3A (K122). Anti-Formyl-HIST1H3A (K122) Antibody (5T153) can be used in ELISA, IHC.

Anti-KAT8 Antibody (3T217) is an antibody targeting KAT8. Anti-KAT8 Antibody (3T217) can be used in ELISA, IHC, IF.

Anti-DEK Antibody (3M77) is an antibody targeting DEK. Anti-DEK Antibody (3M77) can be used in ELISA, IHC, IF, FCM.

<p>Anti-FUBP1 Antibody (1L745) is an antibody targeting FUBP1. Anti-FUBP1 Antibody (1L745) can be used in ELISA, WB, IHC, IF, FCM, IP.</p>

Anti-Histone H2A type 1-B/E Antibody (2D761) is an antibody targeting Histone H2A type 1-B/E. Anti-Histone H2A type 1-B/E Antibody (2D761) can be used in ELISA, WB, IF.

<p>Anti-HNRNPC Antibody (6O738) is an antibody targeting HNRNPC. Anti-HNRNPC Antibody (6O738) can be used in ELISA, WB, IHC, IF, FCM, IP.</p>

Anti-KDM1B Antibody (3U825) is an antibody targeting KDM1B. Anti-KDM1B Antibody (3U825) can be used in ELISA, WB.

<p>Anti-HNRNPK Antibody (2G11) is an antibody targeting HNRNPK. Anti-HNRNPK Antibody (2G11) can be used in ELISA, WB, IHC, IF, IP.</p>

Anti-KDM1A Antibody (4D377) is an antibody targeting KDM1A. Anti-KDM1A Antibody (4D377) can be used in ELISA, WB, IHC.

Anti-Histone H3.1 Antibody (8Z170) is an antibody targeting Histone H3.1. Anti-Histone H3.1 Antibody (8Z170) can be used in ELISA, WB, IHC, IF, FCM.

Anti-Flap endonuclease 1/FEN-1 Antibody (6P187) is an antibody targeting Flap endonuclease 1/FEN-1. Anti-Flap endonuclease 1/FEN-1 Antibody (6P187) can be used in ELISA, WB, IHC, IF.

Anti-HDAC6 Antibody (2F772) is an antibody targeting HDAC6. Anti-HDAC6 Antibody (2F772) can be used in ELISA, WB, IHC, IP.

Anti-Histone H1.0 Antibody (4W4) is an antibody targeting Histone H1.0. Anti-Histone H1.0 Antibody (4W4) can be used in ELISA.

Anti-HIST1H1C Antibody (4V621) is an antibody targeting HIST1H1C. Anti-HIST1H1C Antibody (4V621) can be used in ELISA, IHC, IF, FCM.

Anti-Hydroxyl-Histone H2A type 1-B/E (Y39) Antibody (2P828) is an antibody targeting Hydroxyl-Histone H2A type 1-B/E (Y39). Anti-Hydroxyl-Histone H2A type 1-B/E (Y39) Antibody (2P828) can be used in ELISA, WB.

Anti-HMGB1 Antibody (2H703) is an antibody targeting HMGB1. Anti-HMGB1 Antibody (2H703) can be used in ELISA, IHC, IF, FCM.

Anti-CDC45 Antibody (8Z278) is an antibody targeting CDC45. Anti-CDC45 Antibody (8Z278) can be used in ELISA.

Anti-CDX1 Antibody (3C463) is an antibody targeting CDX1. Anti-CDX1 Antibody (3C463) can be used in ELISA, WB, IF Recommended dilution: WB:1:500-1:2000, IF:1:50-1:200.

Anti-CDC5L Antibody (9X496) is an antibody targeting CDC5L. Anti-CDC5L Antibody (9X496) can be used in ELISA, WB, IHC, IF, IP.

Anti-Mono-methyl-Histone H3.1 (Lys18) Antibody (6N303) is an antibody targeting Mono-methyl-Histone H3.1 (Lys18). Anti-Mono-methyl-Histone H3.1 (Lys18) Antibody (6N303) can be used in ELISA, WB, ICC, IF.

Anti-Phospho-PRKDC (Ser2056) Antibody (3F632) is an antibody targeting Phospho-PRKDC (Ser2056). Anti-Phospho-PRKDC (Ser2056) Antibody (3F632) can be used in ELISA, IF.

Anti-Mono/Di/Tri-methyl-Histone H3.1 (Lys79) Antibody (9Y141) is an antibody targeting Mono/Di/Tri-methyl-Histone H3.1 (Lys79). Anti-Mono/Di/Tri-methyl-Histone H3.1 (Lys79) Antibody (9Y141) can be used in ELISA.

Anti-CD63 Antibody (4G617) is a Mouse antibody targeting CD63. Anti-CD63 Antibody (4G617) can be used in ELISA, WB, IHC, IF, FCM.

Anti-BRIP1 Antibody (9H980) is an antibody targeting BRIP1. Anti-BRIP1 Antibody (9H980) can be used in ELISA, WB.

Anti-CBX2 Antibody (6H584) is an antibody targeting CBX2. Anti-CBX2 Antibody (6H584) can be used in ELISA, WB.

Anti-Di-methyl-Histone H3.1 (Lys4) Antibody (4I767) is an antibody targeting Di-methyl-Histone H3.1 (Lys4). Anti-Di-methyl-Histone H3.1 (Lys4) Antibody (4I767) can be used in ELISA, WB, ICC, IF, FCM.

Anti-Mono-methyl-Histone H3.1 (Arg128) Antibody (8D590) is an antibody targeting Mono-methyl-Histone H3.1 (Arg128). Anti-Mono-methyl-Histone H3.1 (Arg128) Antibody (8D590) can be used in ELISA, WB.

Anti-Acetyl-Histone H4 (Lys5) Antibody (5O810) is an antibody targeting Acetyl-Histone H4 (Lys5). Anti-Acetyl-Histone H4 (Lys5) Antibody (5O810) can be used in ELISA, WB, ICC, IF.