General Ret(Retinol) ELISA Kit

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Retinol (Ret) in serum, plasma and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General Retinol (Ret) in samples from serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species.

Description: A competitive Inhibition ELISA kit for detection of Retinol from General in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: A Rabbit polyclonal antibody against General Retinol (Ret)

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with PE.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with HRP.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with APC.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with Cy3.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with FITC.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with Biotin.

Description: A Rabbit polyclonal antibody against General Retinol (Ret). This antibody is labeled with APC-Cy7.

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Ret protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Ret. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Ret in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Ret protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Ret. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Ret in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human Ret protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Ret. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Ret in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human Ret protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Ret. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Ret in the samples is then determined by comparing the OD of the samples to the standard curve.