General DC(Deoxycholate) ELISA Kit

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General Deoxycholate (DC) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids with no significant corss-reactivity with analogues from other species.

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

Description: A Rabbit polyclonal antibody against General Deoxycholate (DC)

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

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

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

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

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

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

Description: A Rabbit polyclonal antibody against General Deoxycholate (DC). 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 DC protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to DC. 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 DC 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 DC protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to DC. 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 DC in the samples is then determined by comparing the OD of the samples to the standard curve.