Quantifiction of human PBMC
Stimulated sample: Human peripheral blood mononuclear cells (PBMCs) were stimulated with 10 ng/mL PMA for 24h, and the average concentration of IL-2 in the supernatant was measured to be 9219.37 pg/mL.
Unstimulated sample: Human PBMCs were cultured for 24h, and the average concentration of IL-2 in the supernatant was measured to be 1.84 pg/mL.
Product Details
Product Details
Product Specification
| Antigen | IFN-γ |
| Reactivity | Human |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8°C as supplied. |
Kit
| Precision | Intra-assay: 5%; Inter-assay: 10% |
| Sample type | Serum; Plasma; Cell culture supernatant |
| Assay type | Sandwich (quantitative) |
| Sensitivity | 0.5 pg/mL |
| Range | 2.08 pg/mL-8500 pg/mL |
| Recovery | Plasma: 115% Serum: 94% Cell culture supernatant: 118% |
| Assay time | 70 minutes |
| Species reactivity | Human |
Background
Interferon gamma (IFN-γ) is a cytokine critical to both innate and adaptive immunity, and functions as the primary activator of macrophages, in addition to stimulating natural killer cells and neutrophils. A non-IgE-mediated anaphylactic reaction and severe bronchospasm have been reported once after the first injection of interferon gamma. IFN-γ activates cells via a different receptor than IFN-α and IFN-β, which accounts for the different physiological properties of the proteins. Production of IFN-γ is largely restricted to activated CD4+ TH1 T cells, CD8+ T cells, and natural killer cells. One of the most important consequences of IFN-γ secretion is the activation of macrophages. In addition, IFN-γ plays a central role in inflammatory responses by activating endothelial cells, promoting TH1 cell development and cellular immune responses, and up-regulation of major histocompatability complex protein expression on antigen-presenting cells.
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CBA
Linearity
The high-concentration human IL-2 protein was serially diluted using plasma, serum and cell culture supernatant matrices respectively. Then, the concentration of human IL-2 was determined and interpolated based on the target standard curve, and the sample dilution was corrected.
Protocol Diagram
