Human Clusterin ELISA Kit
$350.00 – $450.00
SPECIES | Human |
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Sample Type | Serum, plasma, cell culture supernatant, and other biological samples |
Sample Volume | 100 μL (diluent) |
Sensitivity | 8.38 pg/mL |
Range | 0.25 ng/mL – 16 ng/mL |
Assay Time | 3.5 h |
Recovery | 76% – 117% |
Average Recovery | 0.98 |
Sample Type | Serum, plasma, cell culture supernatant, and other biological samples |
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Sample Volume | 100 μL (diluent) |
Sensitivity | 8.38 pg/mL |
Range | 0.25 ng/mL – 16 ng/mL |
Assay Time | 3.5 h |
Recovery | 76% – 117% |
Average Recovery | 0.98 |
Intra Precision | 3.8 % – 6.2% |
Inter-Precision | 6.9 % – 9.0% |
Platform | ELISA |
Plate | Detachable 96-well plate |
Size | 96T/48T |
Storage | If the reagent kit is unopened, it should be stored at 4℃. However, if it has been opened, the standard solution should be stored at -20℃, while the other components should be stored at 4℃. |
Delivery | 4℃ blue ice transportation |
Components | 96-well polystyrene enzyme-linked immunosorbent assay (ELISA) plate coated with mouse anti-human Clusterin capture antibody Human Clusterin freeze-dried standard Human Clusterin detect Antibody Streptavidin-HRP Assay Buffer(10×) Substrate TMB Stop Solution Washing Buffer(20×) Sealing Film Standard Diluent |
Assay Principle | This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human Clusterin antibodies are precoated on a high-affinity ELISA plate. Standard samples, test samples, and biotinylated detection antibodies are added to the wells of the ELISA plate. After incubation, Clusterin present in the samples binds to the solid-phase antibodies and the detection antibodies. After washing to remove unbound substances, streptavidin-HRP labeled with horseradish peroxidase is added. After washing, a colorimetric substrate, TMB, is added and the plate is incubated in the dark for color development. The intensity of the color reaction is directly proportional to the concentration of Clusterin in the samples.A stop solution is added to terminate the reaction, and the absorbance value is measured at a wavelength of 450 nm (with a reference wavelength range of 570-630 nm). |