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Human LH ELISA Kit
$350.00 – $450.00
| SPECIES | Human |
|---|---|
| Sample Type | Serum, plasma, cell culture supernatant, and other biological samples |
| Sample Volume | 80 μL 1×Assay Buffer and 20 μL sample |
| Sensitivity | 3.17 pg/mL |
| Range | 93.75 pg/mL – 6000 pg/mL |
| Assay Time | 3.5 h |
| Recovery | 92% – 118% |
| Average Recovery | 1.11 |
| Sample Type | Serum, plasma, cell culture supernatant, and other biological samples |
|---|---|
| Sample Volume | 80 μL 1×Assay Buffer and 20 μL sample |
| Sensitivity | 3.17 pg/mL |
| Range | 93.75 pg/mL – 6000 pg/mL |
| Assay Time | 3.5 h |
| Recovery | 92% – 118% |
| Average Recovery | 1.11 |
| Intra Precision | 4.5% – 4.9% |
| Inter-Precision | 4.6% – 4.8% |
| 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-LH monoclonal antibody LH freeze-dried standard LH 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 LH 单克隆 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, LH 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, the TMB chromogenic substrate is added, and color development is carried out while avoiding light. The intensity of the color reaction is directly proportional to the concentration of LH 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). |
