latex beads Search Results


94
Cayman Chemical igg fitc conjugated latex bead phagocytosis assay kit
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Igg Fitc Conjugated Latex Bead Phagocytosis Assay Kit, supplied by Cayman Chemical, 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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Magsphere carboxylic blue latex beads cab400nm
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Carboxylic Blue Latex Beads Cab400nm, supplied by Magsphere, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Polysciences inc latex beads (1:5,000)
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Beads (1:5,000), supplied by Polysciences inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bangs Laboratories latex beads
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Beads, supplied by Bangs Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bangs Laboratories protein a polystyrene microspheres bangs laboratories
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Protein A Polystyrene Microspheres Bangs Laboratories, supplied by Bangs Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cayman Chemical latex beads-rabbit igg-fitc
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Beads Rabbit Igg Fitc, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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PolyScience latex beads
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Beads, supplied by PolyScience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Polysciences inc fitcfluorescent diameter latex beads
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Fitcfluorescent Diameter Latex Beads, supplied by Polysciences inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson fluorescent latex counting beads becton dickinson
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Fluorescent Latex Counting Beads Becton Dickinson, 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
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Polysciences inc latex (2- m diameter) beads
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex (2 M Diameter) Beads, supplied by Polysciences inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Blackwell Science Ltd latex bead-containing phagosomes
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Bead Containing Phagosomes, supplied by Blackwell Science Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Diagnostica Stago latex immunoassay liatest d-di
a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of <t>FITC-labeled</t> <t>IgG-opsonized</t> latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .
Latex Immunoassay Liatest D Di, supplied by Diagnostica Stago, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of FITC-labeled IgG-opsonized latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .

Journal: bioRxiv

Article Title: Recombinant BCG overexpressing a STING agonist elicits trained immunity and improved antitumor efficacy in non-muscle invasive bladder cancer

doi: 10.1101/2020.04.25.061531

Figure Lengend Snippet: a . Percentages of M1- and M2-macrophages and M-MDSCs arising from primary murine macrophages. b . Percentages of inflammatory, TNF-α+ M1, and IL-6 + M1 macrophages, and c . M2 and IL-10 + M2 macrophages arising from primary human macrophages. Data were collected after 24 hr exposures at MOI of 20:1 as determined by flow cytometry using gating schemes shown in Fig. S8-S13 . Data are SEM (n = 3 replicates). d . Phagocytic activity in human primary macrophages in representative confocal photomicrographs showing intracellular uptake of FITC-labeled IgG-opsonized latex beads (green) with nuclei stained blue. e . Autophagy induction and f . quantification by BCG-LC3B colocalization in primary murine macrophages shown by representative confocal photomicrographs. Autophagy was measured by LC3B puncta or g . p62 colocalization with BCG appearing in yellow. FITC-labeled BCG strains are stained green, LC3B or p62 autophagic puncta (red), and nuclei blue. h . Quantification of BCG-p62 colocalization. Cells were fixed using 4% paraformaldehyde 6 h after infection (MOI 10:1), and images obtained with an LSM700 confocal microscope and Fiji software processing. Quantification was by mean fluorescence intensity. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by 2-tailed Student’s t-test. Data shown are for BCG-Tice; similar findings were observed for BCG-Pasteur as shown in Fig. S9 and S11 .

Article Snippet: IgG-FITC conjugated latex bead phagocytosis assay kit (Item No. 500290, Cayman Chemicals, USA) was used for phagocytosis studies.

Techniques: Flow Cytometry, Activity Assay, Labeling, Staining, Infection, Microscopy, Software, Fluorescence