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Manufacture of EVs with functional, surface-displayed IL-12. ( A ) Representative images of IL-12 EVs and control EVs characterized by flow cytometry (independent experiments with n = 3). ( B ) Annexin A1 and IL-12 <t>p70</t> expression in EVs was detected by western blotting (independent experiments with n = 3). ( C ) The IL-12 concentrations in EVs were quantified via ELISA, and the mean IL-12 concentration of IL-12 EVs was 1887 pg/mL (independent experiments with n = 3). D ) IL-12 EVs were stored at − 80 °C, and their concentration was determined by ELISA analysis at different time points (independent experiments with n = 3). ( E ) Representative dose‒response curves of IFN-γ secretion from T cells (cell density: 1*10 6 /mL) after treatment with doses of rhIL-12 or IL-12 EVs. The EC50 values derived from the graphs were 54.9 pg/mL and 9.4 pg/mL, respectively (independent experiments with n = 3). Data are presented as mean ± SEM. Statistical analysis was performed using unpaired t test. **** p < 0.0001
Anti Il 12 P70 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Manufacture of EVs with functional, surface-displayed IL-12. ( A ) Representative images of IL-12 EVs and control EVs characterized by flow cytometry (independent experiments with n = 3). ( B ) Annexin A1 and IL-12 <t>p70</t> expression in EVs was detected by western blotting (independent experiments with n = 3). ( C ) The IL-12 concentrations in EVs were quantified via ELISA, and the mean IL-12 concentration of IL-12 EVs was 1887 pg/mL (independent experiments with n = 3). D ) IL-12 EVs were stored at − 80 °C, and their concentration was determined by ELISA analysis at different time points (independent experiments with n = 3). ( E ) Representative dose‒response curves of IFN-γ secretion from T cells (cell density: 1*10 6 /mL) after treatment with doses of rhIL-12 or IL-12 EVs. The EC50 values derived from the graphs were 54.9 pg/mL and 9.4 pg/mL, respectively (independent experiments with n = 3). Data are presented as mean ± SEM. Statistical analysis was performed using unpaired t test. **** p < 0.0001
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List of antibodies used for monocyte flow cytometry
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Sorted naïve CD8 T cells were activated with CD3/CD28 beads for 24 hours, rested for 2 days and restimulated with CD3/CD28 beads for 8 days in the presence of the indicated cytokines with or without TGF-β. a Data from a representative donor and ( b ) summary of NKG2A expression after 8 days of culture are shown ( n = 5). c Expression of NKG2A by CD8 T cells after stimulation of PBMC with SEB in the presence of isotype control, <t>α-IL-12p70</t> Ab, α-CD40 Ab or both. Data from one representative donor are shown. d Summary of ( c ) (left) and percentage inhibition of NKG2A expression by CD8 T cells in the different culture conditions (right) ( n = 4). e Detection of IL-12p70 in the culture supernatants of PBMCs stimulated for 3 days with SEB in presence or not of α-CD40 Ab (left) and percentage inhibition of IL-12p70 secretion (right) ( n = 3). b , d , e Data are from distinct healthy donors. Horizontal lines indicate the mean ± SEM. NS= non-significant; p -values were determined by one-way ANOVA with Tukey’s post hoc test ( b , d , g ).
Anti Human Il 12p70, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems cd40l blocking
Sorted naïve CD8 T cells were activated with CD3/CD28 beads for 24 hours, rested for 2 days and restimulated with CD3/CD28 beads for 8 days in the presence of the indicated cytokines with or without TGF-β. a Data from a representative donor and ( b ) summary of NKG2A expression after 8 days of culture are shown ( n = 5). c Expression of NKG2A by CD8 T cells after stimulation of PBMC with SEB in the presence of isotype control, <t>α-IL-12p70</t> Ab, α-CD40 Ab or both. Data from one representative donor are shown. d Summary of ( c ) (left) and percentage inhibition of NKG2A expression by CD8 T cells in the different culture conditions (right) ( n = 4). e Detection of IL-12p70 in the culture supernatants of PBMCs stimulated for 3 days with SEB in presence or not of α-CD40 Ab (left) and percentage inhibition of IL-12p70 secretion (right) ( n = 3). b , d , e Data are from distinct healthy donors. Horizontal lines indicate the mean ± SEM. NS= non-significant; p -values were determined by one-way ANOVA with Tukey’s post hoc test ( b , d , g ).
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Image Search Results


Manufacture of EVs with functional, surface-displayed IL-12. ( A ) Representative images of IL-12 EVs and control EVs characterized by flow cytometry (independent experiments with n = 3). ( B ) Annexin A1 and IL-12 p70 expression in EVs was detected by western blotting (independent experiments with n = 3). ( C ) The IL-12 concentrations in EVs were quantified via ELISA, and the mean IL-12 concentration of IL-12 EVs was 1887 pg/mL (independent experiments with n = 3). D ) IL-12 EVs were stored at − 80 °C, and their concentration was determined by ELISA analysis at different time points (independent experiments with n = 3). ( E ) Representative dose‒response curves of IFN-γ secretion from T cells (cell density: 1*10 6 /mL) after treatment with doses of rhIL-12 or IL-12 EVs. The EC50 values derived from the graphs were 54.9 pg/mL and 9.4 pg/mL, respectively (independent experiments with n = 3). Data are presented as mean ± SEM. Statistical analysis was performed using unpaired t test. **** p < 0.0001

Journal: Experimental Hematology & Oncology

Article Title: Improving CAR-T cell function through a targeted cytokine delivery system utilizing car target-modified extracellular vesicles

doi: 10.1186/s40164-025-00701-z

Figure Lengend Snippet: Manufacture of EVs with functional, surface-displayed IL-12. ( A ) Representative images of IL-12 EVs and control EVs characterized by flow cytometry (independent experiments with n = 3). ( B ) Annexin A1 and IL-12 p70 expression in EVs was detected by western blotting (independent experiments with n = 3). ( C ) The IL-12 concentrations in EVs were quantified via ELISA, and the mean IL-12 concentration of IL-12 EVs was 1887 pg/mL (independent experiments with n = 3). D ) IL-12 EVs were stored at − 80 °C, and their concentration was determined by ELISA analysis at different time points (independent experiments with n = 3). ( E ) Representative dose‒response curves of IFN-γ secretion from T cells (cell density: 1*10 6 /mL) after treatment with doses of rhIL-12 or IL-12 EVs. The EC50 values derived from the graphs were 54.9 pg/mL and 9.4 pg/mL, respectively (independent experiments with n = 3). Data are presented as mean ± SEM. Statistical analysis was performed using unpaired t test. **** p < 0.0001

Article Snippet: For EV molecule characterization, the membranes were incubated overnight at 4 °C with the following antibodies on a shaker: an anti-Annexin A1 antibody (Abcam, ab214486, 1:2000), and anti-IL-12 p70 antibody (R&D Systems, MAB219-SP, 1:1000).

Techniques: Functional Assay, Control, Flow Cytometry, Expressing, Western Blot, Enzyme-linked Immunosorbent Assay, Concentration Assay, Derivative Assay

List of antibodies used for monocyte flow cytometry

Journal: The Journal of Clinical Endocrinology and Metabolism

Article Title: Magnesium Supplementation Modulates T-cell Function in People with Type 2 Diabetes and Low Serum Magnesium Levels

doi: 10.1210/clinem/dgae097

Figure Lengend Snippet: List of antibodies used for monocyte flow cytometry

Article Snippet: IL12 (p40/p70) , Miltenyi , 130-123-312 , AB_2921743.

Techniques:

Percentage of IL6 (A), IL-1β (B), TNF (C), and IL12 producing CD14 + monocytes (D) under pathogenic stimulation after treatment with placebo (white) and magnesium (gray). S. Aureus, Staphylococcus aureus ; Mtb, Mycobacterium tuberculosis . Data are presented as median and individual values.

Journal: The Journal of Clinical Endocrinology and Metabolism

Article Title: Magnesium Supplementation Modulates T-cell Function in People with Type 2 Diabetes and Low Serum Magnesium Levels

doi: 10.1210/clinem/dgae097

Figure Lengend Snippet: Percentage of IL6 (A), IL-1β (B), TNF (C), and IL12 producing CD14 + monocytes (D) under pathogenic stimulation after treatment with placebo (white) and magnesium (gray). S. Aureus, Staphylococcus aureus ; Mtb, Mycobacterium tuberculosis . Data are presented as median and individual values.

Article Snippet: IL12 (p40/p70) , Miltenyi , 130-123-312 , AB_2921743.

Techniques:

Sorted naïve CD8 T cells were activated with CD3/CD28 beads for 24 hours, rested for 2 days and restimulated with CD3/CD28 beads for 8 days in the presence of the indicated cytokines with or without TGF-β. a Data from a representative donor and ( b ) summary of NKG2A expression after 8 days of culture are shown ( n = 5). c Expression of NKG2A by CD8 T cells after stimulation of PBMC with SEB in the presence of isotype control, α-IL-12p70 Ab, α-CD40 Ab or both. Data from one representative donor are shown. d Summary of ( c ) (left) and percentage inhibition of NKG2A expression by CD8 T cells in the different culture conditions (right) ( n = 4). e Detection of IL-12p70 in the culture supernatants of PBMCs stimulated for 3 days with SEB in presence or not of α-CD40 Ab (left) and percentage inhibition of IL-12p70 secretion (right) ( n = 3). b , d , e Data are from distinct healthy donors. Horizontal lines indicate the mean ± SEM. NS= non-significant; p -values were determined by one-way ANOVA with Tukey’s post hoc test ( b , d , g ).

Journal: Nature Communications

Article Title: IL-12 drives the expression of the inhibitory receptor NKG2A on human tumor-reactive CD8 T cells

doi: 10.1038/s41467-024-54420-w

Figure Lengend Snippet: Sorted naïve CD8 T cells were activated with CD3/CD28 beads for 24 hours, rested for 2 days and restimulated with CD3/CD28 beads for 8 days in the presence of the indicated cytokines with or without TGF-β. a Data from a representative donor and ( b ) summary of NKG2A expression after 8 days of culture are shown ( n = 5). c Expression of NKG2A by CD8 T cells after stimulation of PBMC with SEB in the presence of isotype control, α-IL-12p70 Ab, α-CD40 Ab or both. Data from one representative donor are shown. d Summary of ( c ) (left) and percentage inhibition of NKG2A expression by CD8 T cells in the different culture conditions (right) ( n = 4). e Detection of IL-12p70 in the culture supernatants of PBMCs stimulated for 3 days with SEB in presence or not of α-CD40 Ab (left) and percentage inhibition of IL-12p70 secretion (right) ( n = 3). b , d , e Data are from distinct healthy donors. Horizontal lines indicate the mean ± SEM. NS= non-significant; p -values were determined by one-way ANOVA with Tukey’s post hoc test ( b , d , g ).

Article Snippet: For IL-12p70 and CD40L blocking experiments, anti-Human Il-12p70 (R&D Systems, cat #MAB219-100, 10 μg/ml final), anti-CD40 (BioLegend, cat #313019, clone HB14, 10 μg/ml final) or isotype control mouse IgG1 (BioLegend, cat #400166, clone MOPC21, 10 μg/ml final) were added in the corresponding wells.

Techniques: Expressing, Control, Inhibition