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Mouse ifn γ elisa kit

Manufactured by Elabscience

The Mouse IFN-γ ELISA Kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) designed for the measurement of mouse interferon-gamma (IFN-γ) levels in biological samples such as cell culture supernatants, serum, and plasma.

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5 protocols using mouse ifn γ elisa kit

1

Measuring Mouse IFN-γ Levels

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IFN-γ levels were measured using a mouse IFN-γ ELISA kit (Elabscience), as described by the manufacturer.
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2

Mouse Serum IFN-γ Quantification

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The level of IFN-γ in mouse serum was analyzed using the Mouse IFN-γ ELISA Kit (Elabscience, Wuhan, China) according to the manufacturer’s instructions.
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3

Serum Inflammatory Factors ELISA Assay

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Serum matrix metalloproteinase-9 (MMP-9) and inflammatory factors, including interleukins-12 (IL-12), IL-10, interferon-γ (IFN-γ), and IL-4, were measured using the following ELISA kits (Elabscience): Mouse MMP-9 ELISA kit (Cat No. E-EL-M3052), Mouse IL-12 ELISA kit (Cat No. E-EL-M0726c), Mouse IL-10 ELISA kit (Cat No. E-EL-M0046c), Mouse IFN-γ ELISA kit (Cat No. E-EL-M0048c), and Mouse IL-4 ELISA kit (Cat No. E-EL-M0043c). All procedures followed the manufacturer's instructions.
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4

Cytokine Quantification in Tumor Tissues

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For in vivo assays, tumor tissues were minced, homogenized, and subjected to beads heating in PBS with protease inhibitor cocktail (K1007, APExBIO) on day 3 or day 6 after completion of treatment. For in vitro tests, culture media were collected by centrifugation. Quantification of cytokines in tumors and media was performed by Mouse IL-12 ELISA Kit (M1270, R&D) and Mouse IFN-γ ELISA Kit (E-EL-M0048c, Elabscience) following the manufacturer’s instruction, respectively.
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5

Inhibiting CD8+ T cell glycolysis

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The method for CD8+ T cell sorting and co-culturing was the same as described previously. For the inhibition of CD8+ T cell glycolysis, AZ-PFKFB3-67 (MedChemExpress, USA) was used at the concentration of 5μM, 10 μM and 20μM respectively for 24h after cell sorting and for another 24 hours after glucose supplementation. The culture supernatant was collected, and the content of IFN-γ was measured using Mouse IFN-γ ELISA Kit (Elabscience, Wuhan).
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