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Human IFN-γ Single Plex Kit (Flow Cytometry Bead Assay)

Human IFN-γ Single Plex Kit (Flow Cytometry Bead Assay)

Catalog Number: S0Q3005 Reactivity: Human Conjugation: Brand: Starter
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Regular price $500 USD
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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.

Picture

CBA

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.

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