General 2-AG(2-Arachidonoylglycerol) ELISA Kit

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General 2-Arachidonoylglycerol (2-AG) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General 2-Arachidonoylglycerol (2-AG) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General 2-Arachidonoylglycerol (2-AG) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General 2-Arachidonoylglycerol (2-AG) in serum, plasma and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General 2-Arachidonoylglycerol (2-AG) 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 2-Arachidonoylglycerol from General in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with 2-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 2-AG. 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 2-AG 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 2-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 2-AG. 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 2-AG 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 2-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human 2-AG. 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 2-AG 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 2-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human 2-AG. 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 2-AG in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: Description of target: ;Species reactivity: Pan-Species;Application: ;Assay info: Assay Methodology: Competitive Inhibition Immunoassay;Sensitivity: 1.41 ng/mL

Description: 2-Arachidonoylglycerol

Description: 2-Arachidonoylglycerol

Description: 2-Arachidonoylglycerol

Description: 2-Arachidonoylglycerol

Description: 2-Arachidonoylglycerol