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UniPlex Human CAR-TCRS Cytokine Multiplex OneStep ELISA Kit (IL-2, IL-6, TNF-a, IFN-γ)

UniPlex Human CAR-TCRS Cytokine Multiplex OneStep ELISA Kit (IL-2, IL-6, TNF-a, IFN-γ)

Catalog Number: S0C3801 Reactivity: Hu Conjugation: Brand: Starter
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Regular price $1,335 USD
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Product Details

Product Specification


Immunogen Recombinant Protein
Antibody Type Recombinant mAb
Reactivity Hu
Purification Protein A
Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8°C as supplied.

Kit


Sample type Cell culture supernatant; Serum; Plasma
Assay type Sandwich (quantitative)
Range Human IL-2: 7.81 pg/mL – 500 pg/mL
Human IL-6: 0.78 pg/mL – 50 pg/mL
Human TNF-α: 7.81 pg/mL – 500 pg/mL
Human IFN-γ: 3.13 pg/mL – 200 pg/mL
Recovery Human IFN-γ
Assay time 60 minutes
Species reactivity Hu

Background

Human IL-2, IL-6, TNF-α, and IFN-γ are key cytokines that orchestrate diverse immune functions, ranging from T cell regulation to inflammation and antimicrobial defense. IL-2, produced mainly by activated T cells, drives T cell proliferation and supports regulatory T cell survival, making it critical for immune homeostasis and cancer immunotherapy. IL-6 is a pleiotropic cytokine secreted by immune and stromal cells; it induces acute-phase responses and B cell differentiation but can also fuel chronic inflammation and cytokine storms when dysregulated. TNF-α, a major pro-inflammatory cytokine from macrophages and T cells, mediates fever, apoptosis, and cachexia, and is a primary therapeutic target in autoimmune diseases such as rheumatoid arthritis. IFN-γ, the sole type II interferon, is produced by natural killer cells and T lymphocytes; it activates macrophages, enhances antigen presentation, and directs cell-mediated immunity against intracellular pathogens. Together, these four cytokines form an interconnected network that balances immune activation, inflammation, and host defense.

Picture

ELISA

Standard curve
Example of Human IL-2 standard curve in Assay Diluent G1.

Standard curve
Example of Human IL-6 standard curve in Assay Diluent G1.

Standard curve
Example of Human TNF-α standard curve in Assay Diluent G1.

Standard curve
Example of Human IFN-γ standard curve in Assay Diluent G1.

Linearity
The concentrations of Human IL-2 were measured and interpolated from the target standard curves and corrected for sample dilution.
The sample is undiluted samples are as follows:  Jurkat T cells stimulated with 10 ng/ml PMA and 150 ng/ml A23187 for 24 h (10%). The interpolated dilution factor corrected values are plotted. The mean target concentration was determined to be 3160.45 pg/mL in stimulated Jurkat supernatant.

Linearity
The concentrations of Human IL-6 were measured and interpolated from the target standard curves and corrected for sample dilution.
The sample is undiluted samples are as follows:  human PBMC cells stimulated with 10ug/ml PHA for 5 days (0.16%). The interpolated dilution factor corrected values are plotted. The mean target concentration was determined to be 38252.05 pg/mL in stimulated human PBMC supernatant.

Linearity
The concentrations of Human TNF-α were measured and interpolated from the target standard curves and corrected for sample dilution.
The sample is undiluted samples are as follows:  human PBMC cells stimulated with 10ug/ml PHA for 5 days (10%). The interpolated dilution factor corrected values are plotted. The mean target concentration was determined to be 6362.08 pg/mL in stimulated human PBMC supernatant.

Linearity
The concentrations of Human IFN-γ were measured and interpolated from the target standard curves and corrected for sample dilution.
The sample is undiluted samples are as follows:  human PBMC cells stimulated with 10ug/ml PHA for 5 days (2.5%). The interpolated dilution factor corrected values are plotted. The mean target concentration was determined to be 10054.28 pg/mL in stimulated human PBMC supernatant.

Consistency rate
The concordance rate between biological sample concentrations calculated from standard curves based on the kit-recommended high and low concentrations versus those calculated from the full standard curve.

Protocol Diagram