anti ifnγ neutralizing antibody Search Results


human ifn-gamma antibody  (Bio-Techne corporation)
92
Bio-Techne corporation human ifn-gamma antibody
Human Ifn Gamma Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human ifn-gamma antibody/product/Bio-Techne corporation
Average 92 stars, based on 1 article reviews
human ifn-gamma antibody - by Bioz Stars, 2026-04
92/100 stars
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anti-ifn–γ neutralizing antibody clone 133.5  (Bio X Cell)
90
Bio X Cell anti-ifn–γ neutralizing antibody clone 133.5
Anti Ifn–γ Neutralizing Antibody Clone 133.5, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-ifn–γ neutralizing antibody clone 133.5/product/Bio X Cell
Average 90 stars, based on 1 article reviews
anti-ifn–γ neutralizing antibody clone 133.5 - by Bioz Stars, 2026-04
90/100 stars
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neutralizing anti-ifn- γ monoclonal antibody  (Becton Dickinson)
90
Becton Dickinson neutralizing anti-ifn- γ monoclonal antibody
Role of <t>IFN-γ</t> on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml <t>anti-IFN-γ</t> neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).
Neutralizing Anti Ifn γ Monoclonal Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/neutralizing anti-ifn- γ monoclonal antibody/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
neutralizing anti-ifn- γ monoclonal antibody - by Bioz Stars, 2026-04
90/100 stars
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monoclonal antibodies (mabs) h22 (neutralizing anti-murine ifnγ)  (Leinco Technologies)
90
Leinco Technologies monoclonal antibodies (mabs) h22 (neutralizing anti-murine ifnγ)
Role of <t>IFN-γ</t> on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml <t>anti-IFN-γ</t> neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).
Monoclonal Antibodies (Mabs) H22 (Neutralizing Anti Murine Ifnγ), supplied by Leinco Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/monoclonal antibodies (mabs) h22 (neutralizing anti-murine ifnγ)/product/Leinco Technologies
Average 90 stars, based on 1 article reviews
monoclonal antibodies (mabs) h22 (neutralizing anti-murine ifnγ) - by Bioz Stars, 2026-04
90/100 stars
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neutralizing anti-ifn-γ ebioscience xmg1.2  (Thermo Fisher)
90
Thermo Fisher neutralizing anti-ifn-γ ebioscience xmg1.2
Role of <t>IFN-γ</t> on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml <t>anti-IFN-γ</t> neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).
Neutralizing Anti Ifn γ Ebioscience Xmg1.2, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/neutralizing anti-ifn-γ ebioscience xmg1.2/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
neutralizing anti-ifn-γ ebioscience xmg1.2 - by Bioz Stars, 2026-04
90/100 stars
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human anti-ifn-γ neutralizing antibodies  (Amgen)
90
Amgen human anti-ifn-γ neutralizing antibodies
Role of <t>IFN-γ</t> on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml <t>anti-IFN-γ</t> neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).
Human Anti Ifn γ Neutralizing Antibodies, supplied by Amgen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human anti-ifn-γ neutralizing antibodies/product/Amgen
Average 90 stars, based on 1 article reviews
human anti-ifn-γ neutralizing antibodies - by Bioz Stars, 2026-04
90/100 stars
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neutralization antibody anti-ifn-γ  (PeproTech)
90
PeproTech neutralization antibody anti-ifn-γ
Role of <t>IFN-γ</t> on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml <t>anti-IFN-γ</t> neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).
Neutralization Antibody Anti Ifn γ, supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/neutralization antibody anti-ifn-γ/product/PeproTech
Average 90 stars, based on 1 article reviews
neutralization antibody anti-ifn-γ - by Bioz Stars, 2026-04
90/100 stars
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Image Search Results


Role of IFN-γ on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml anti-IFN-γ neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).

Journal:

Article Title: CD40-CD154 interactions between macrophages and natural killer cells during sepsis are critical for macrophage activation and are not interferon gamma dependent

doi: 10.1111/j.1365-2249.2004.02547.x

Figure Lengend Snippet: Role of IFN-γ on NK cell and macrophage (MΦ) activation in single cell-type and mixed-cell coculture. CD69 expression was determined on splenic NK cells isolated from IFN-γ–/– mice after 24 h culture alone or with MΦ from wild type (WT) C57BL/6, with and without LPS (a). Cocultures of NK cells with MΦ (NK + MΦ, NK + MΦ + LPS) showed increases in CD69 expression compared to culture alone (NK, NK + LPS) both with and without LPS, although these levels were significantly decreased from CD69 levels in NK cells from WT mice (compare with Fig. 1a). Phagocytosis level was determined at 48 h in WT MΦ with and without NK cells from IFN-γ–/– mice and with and without LPS (b). There were significant increases in phagocytosis mean channel fluorescence (MCF) of MΦ cocultured with NK cells (MΦ + NK, MΦ + NK + LPS), although these levels were again lower than in WT mice (compare with Figs 1b,c). There were no differences in phagocytosis MCF between MΦ cocultured with NK cells with and without 1 µg/ml anti-IFN-γ neutralizing antibody (c). n = 6 per experimental group and data are representative of separate repeated experiments. Data presented as mean ± s.e.m. * or †P < 0·05, Kruskal–Wallis (CD69 percentages), anova (MCF).

Article Snippet: Macrophages were also cultured with NK cells and 1 µ g/ml of neutralizing anti-IFN- γ monoclonal antibody (BD Pharmingen, San Diego, CA, USA), or with NK cells isolated from IFN- γ –/– mice, to elucidate the role of NK derived IFN- γ on macrophage activation.

Techniques: Activation Assay, Expressing, Isolation, Fluorescence

Levels of IL-6 measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40−/– mice were also used, as well as splenic NK cells from CD154−/– and IFN- γ −/– mice

Journal:

Article Title: CD40-CD154 interactions between macrophages and natural killer cells during sepsis are critical for macrophage activation and are not interferon gamma dependent

doi: 10.1111/j.1365-2249.2004.02547.x

Figure Lengend Snippet: Levels of IL-6 measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40−/– mice were also used, as well as splenic NK cells from CD154−/– and IFN- γ −/– mice

Article Snippet: Macrophages were also cultured with NK cells and 1 µ g/ml of neutralizing anti-IFN- γ monoclonal antibody (BD Pharmingen, San Diego, CA, USA), or with NK cells isolated from IFN- γ –/– mice, to elucidate the role of NK derived IFN- γ on macrophage activation.

Techniques: Enzyme-linked Immunosorbent Assay, Cell Culture

Levels of TNF- α measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40–/– mice were also used, as well as splenic NK cells from CD154–/– and IFN- γ –/– mice

Journal:

Article Title: CD40-CD154 interactions between macrophages and natural killer cells during sepsis are critical for macrophage activation and are not interferon gamma dependent

doi: 10.1111/j.1365-2249.2004.02547.x

Figure Lengend Snippet: Levels of TNF- α measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40–/– mice were also used, as well as splenic NK cells from CD154–/– and IFN- γ –/– mice

Article Snippet: Macrophages were also cultured with NK cells and 1 µ g/ml of neutralizing anti-IFN- γ monoclonal antibody (BD Pharmingen, San Diego, CA, USA), or with NK cells isolated from IFN- γ –/– mice, to elucidate the role of NK derived IFN- γ on macrophage activation.

Techniques: Enzyme-linked Immunosorbent Assay, Cell Culture

Levels of IL-12 measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40−/– mice were also used, as well as splenic NK cells from CD154–/– and IFN- γ –/– mice

Journal:

Article Title: CD40-CD154 interactions between macrophages and natural killer cells during sepsis are critical for macrophage activation and are not interferon gamma dependent

doi: 10.1111/j.1365-2249.2004.02547.x

Figure Lengend Snippet: Levels of IL-12 measured by ELISA in culture supernatant from peritoneal macrophages cultured for 48 h with and without splenic NK cells and with and without 1 µ g/ml LPS. Peritoneal macrophages from CD40−/– mice were also used, as well as splenic NK cells from CD154–/– and IFN- γ –/– mice

Article Snippet: Macrophages were also cultured with NK cells and 1 µ g/ml of neutralizing anti-IFN- γ monoclonal antibody (BD Pharmingen, San Diego, CA, USA), or with NK cells isolated from IFN- γ –/– mice, to elucidate the role of NK derived IFN- γ on macrophage activation.

Techniques: Enzyme-linked Immunosorbent Assay, Cell Culture