Human IL-35 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 | 20 μL |
Sensitivity | 76.93 pg/mL |
Range | 0.47 ng/mL – 30 ng/mL |
Assay Time | 3.5 h |
Recovery | 95% – 119% |
Average Recovery | 1.08 |
Sample Type | Serum, plasma, cell culture supernatant, and other biological samples |
---|---|
Sample Volume | 20 μL |
Sensitivity | 76.93 pg/mL |
Range | 0.47 ng/mL – 30 ng/mL |
Assay Time | 3.5 h |
Recovery | 95% – 119% |
Average Recovery | 1.08 |
Intra Precision | 4.7% – 4.9% |
Inter-Precision | 4.5% – 4.9% |
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 anti-IL-35 monoclonal antibody Human IL-35 freeze-dried standard IL-35 detect Antibody Standard Diluent Assay Buffer(10×) Substrate TMB Stop Solution Washing Buffer(20×) Sealing Film |
Assay Principle | This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human IL-12/IL-35 p35 antibodies are precoated on a high-affinity ELISA plate.Standards and test samples are added to the wells of the ELISA plate. After incubation, the IL-35 present in the samples binds to the solid-phase antibodies. After washing to remove unbound substances, biotinylated detection antibodies are added and incubated. After washing to remove unbound biotinylated antibodies, 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 IL-35 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). |