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Human CCK8(Cholecystokinin 8, Octapeptide) ELISA Kit - Details |
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Sensitivity |
4.46 pg/mL |
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Range |
15.63-1000 pg/mL |
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Alternative Names |
Sincalide |
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Detection Method |
Competitive Inhibition |
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Standard |
1000 pg/mL |
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Sample type |
Serum, plasma, cell lysates, cell culture supernates and other biological fluids |
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Principle |
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human CCK8. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CCK8. 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 sulfuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. |
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Human CCK8(Cholecystokinin 8, Octapeptide) ELISA Kit |
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Sensitivity |
1.2pg/ml |
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Range |
3pg/ml-200pg/ml |
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Detection Method |
Elisa |
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Sample type |
Serum, plasma, Urine samples, Cell samples, Tissue samples and other biological fluids |
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Storage |
2-8℃ |
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Human CCK8(Cholecystokinin 8, Octapeptide) ELISA Kit |
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Sensitivity |
31.25pg/ml |
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Range |
125pg/ml-8000pg/ml |
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Detection Method |
Quantitative Detection |
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Sample type |
with serum, plasma, culture media, or any biological fluids |
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Storage |
2-8℃ |
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Principle |
The quantitative detection of Human CCK-8 antigen is based on the ELISA (Enzyme-Linked Immunosorbent Assay) technique. The microplate wells are pre-coated with an antibody specific to Human CCK-8. After incubation, the corresponding antigen in the sample or standards will bind to the immobilized antibody. After washing the microplate wells to remove all unbound sample material, horseradish peroxidase (HRP) labeled antibody conjugate is added, which binds to the antigen, forming antibody-antigen-enzyme-labeled antibody complex upon incubation. In a second wash step, all unbound material is removed. The immune complex formed by the bound conjugate is visualized by adding Tetramethylbenzidine (TMB) substrate, which gives a blue color reaction in wells containing the complex. A stop solution containing acid terminates the reaction, producing a yellow end-point coloration proportional to the amount of specific antigen present in the sample. Absorbance is measured at 450 nm using an ELISA microwell plate reader. Analysis is completed by comparing the OD values of samples to the standard curve. |
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Human CCK8(Cholecystokinin 8, Octapeptide) ELISA Kit |
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Sensitivity |
25pg/mL |
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Range |
125-8000pg/mL |
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Detection Method |
Sandwich-ELISA |
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Sample type |
with serum, plasma, culture media, Cell lysates or any biological fluids |
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Storage |
2-8℃ |
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Principle |
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human CCK. Samples (or Standards) are added to the micro ELISA plate wells and
combined with the specific antibody. Then a biotinylated detection antibody specific for Human CCK and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human CCK, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Human CCK. You can calculate the concentration of Human CCK in the samples by comparing the OD of the samples to the standard curve. |
