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The kit is developed for quantitative detection of natural and recombinant human IL-7 in serum, plasma and cell culture supernatants.
It is for research use only.
Assay Type | Sandwich-ELISA |
Analyte | IL-7 |
Format | 96-wells plate breakable into 12 x 8 wells strips |
Reactivity | Human |
Sensitivity | 5.0 pg/mL |
Assay Time | 2.75 hr |
Sample volume | 50 μL |
Range | 7.81 pg/mL-500 pg/mL |
Sample Type | For the quantitative determination of human IL-7 in serum, plasma and cell supernatant. |
NIBSC Code | 90/530, NIBSC/WHO (90/530) approximate value (U/mL) = 0.78 x Clinmax Human IL-7 value (pg/mL) |
Elevate your research experience with our Cytokine/Biomarker Detection Kits, where accuracy, reliability, and ease of use are converging to deliver exceptional results.
For each experiment, a standard curve needs to be set for each microplate, and the specific OD value may vary depending on different laboratories, testers, or equipment. The following example data is for reference only. The sample concentration was calculated based on the results of the standard curve. The minimum detectable concentration of IL-7 is less than 5 pg/mL.
Ten replicates of each of three samples containing different IL-7 concentrations were tested in one assay. Acceptable criteria: CV<10%.
Three samples containing different concentrations of IL-7 were tested in inde-pendent assays. Acceptable criteria: CV<15%.
Recombinant IL-7 was spiked into three human serum samples, and then analyzed. The average recovery of IL-7 for serum samples is 95.2%.
ID | Components | Size |
CEA216-C01 | Pre-coated Anti-IL-7 Antibody Microplate | 1 plate |
CEA216-C02 | Human IL-7 Standard | 5 ng×2 |
CEA216-C03 | Biotin-Anti-IL-7 Antibody Con. Solution | 100 μL |
CEA216-C04 | Biotin-Antibody Dilution Buffer | 8 mL |
CEA216-C05 | Streptavidin-HRP Con. Solution | 500 μL |
CEA216-C06 | Streptavidin-HRP Dilution Buffer | 15 mL |
CEA216-C07 | 20×Washing Buffer | 50 mL |
CEA216-C08 | Sample Dilution Buffer | 15 mL×2 |
CEA216-C09 | Substrate Solution | 12 mL |
CEA216-C10 | Stop Solution | 6 mL |
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English Name | Research Code | Research Phase | Company | First Brand Name | First Approved Country | First Indication | First Approved Company | First Approved Date | Indications | Clinical Trials |
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English Name | Research Code | Research Phase | Company | Indications | Clinical Trials |
---|---|---|---|---|---|
Anti-GPC3 chimeric antigen receptor T cell therapy (Hunan Zhaotai Yongren Biotech/Guangdong Zhaotai Invivo Biomedicine) | Phase 1 Clinical | Hunan Zhaotai Yongren Biotech Co Ltd, Guangdong Zhaotai Invivo Biomedicine Co Ltd | Carcinoma, Hepatocellular; Carcinoma, Non-Small-Cell Lung | Details | |
ADP-TILIL7 | ADP-TILIL7 | Phase 1 Clinical | Adaptimmune Therapeutics Plc | Melanoma | Details |
GSK-3888130-B | GSK3888130B; GSK-3888130; GSK-3888130-B | Phase 1 Clinical | Glaxosmithkline Plc | Multiple Sclerosis | Details |
BNT-152 | BNT-152 | Phase 1 Clinical | Biontech Se | Solid tumours | Details |
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