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Limited Edition Golden Llama is here! Check out how you can get one. 
Limited Edition Golden Llama is here! Check out how you can get one.
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The kit is developed for quantitative detection of natural and recombinant human IFN-gamma in serum, plasma and cell culture supernatants.
It is suitable for potency assay of CAR-T/NK cell therapy. It has been calibrated against a highly purified human IFN-γ and is evaluated with standard from NIBSC/WHO. Reference Reagent INTERFERON GAMMA (Human, rDNA derived) NIBSC code: 82/587.
It is for research use only.
| Analyte | IFN-γ |
| Assay Type | Sandwich-ELISA |
| Reactivity | Human |
| Sensitivity | 4pg/mL |
| Range | 7.81 pg/mL-1000 pg/mL |
| Assay Time | 2 hr |
| Sample Type | Cell Culture Supernatants, Plasma, Serum. |
| Sample volume | 50 uL |
| Format | 96-wells plate breakable into 12 x 8 wells strips |
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 IFN-γ is less than 4.0 pg/mL.
Serum - IFN-γ concentrations were measured in 208 human serum samples, which were collected from healthy human subjects. The measurements of 208 samples are shown in the figure below.
3 types of materials were tested to observe if there were matrix effect (interference). If the concentration of hemoglobin (simulated hemolysis) is less than 3500 mg/dL, the concentration of triglyceride (simulated lipid blood) is less than 3.0 mg/mL, and the concentration of bilirubin (simulated jaundice) is less than 20 mg/dL, testing results will not be affected.
According to the hook effect evaluation, tested results will not be affected when IFN-γ concentration is higher than 250 ng/mL.
High concentrations of human IFN-γ serum samples were diluted with 1:2, 1:4, 1:8, 1:16, 1:32 and 1:64 ratios for gradient dilution to evaluate the linearity of the assay. In the serum samples, the average detection rate of IFN-γ was 99.16%.
10 replicates of each of 4 samples containing different IFN-γ concentrations were tested in one assay. Acceptable criteria: CV＜10%.
4 samples containing different concentrations of IFN-γ were tested in the independent assays. Acceptable criteria: CV<15%.
IFN-γ was spiked into 5 human serum samples, and then analyzed. The average recovery of IFN-γ for serum samples is 95.92%.
| ID | Components | Size |
| CEA006-C01 | Pre-coated Anti-IFN-γ Antibody Microplate | 1 plate |
| CEA006-C02 | Human IFN-γ Standard | 14 μg×2 |
| CEA006-C03 | Biotin-Anti-IFN-γ Antibody Con. Solution | 150 μL |
| CEA006-C04 | Biotin-Antibody Dilution Buffer | 8 mL |
| CEA006-C05 | Streptavidin-HRP Con. Solution | 500 μL |
| CEA006-C06 | Streptavidin-HRP Dilution Buffer | 15 mL |
| CEA006-C07 | 20× Washing Buffer | 50 mL |
| CEA006-C08 | Sample Dilution Buffer | 15 mL×2 |
| CEA006-C09 | Substrate Solution | 12 mL |
| CEA006-C10 | Stop Solution | 6 mL |
Price(EUR) : €550.00
Price(EUR) :
Price(EUR) :
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