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Primary and secondary antibodies used in this study
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SVEC4–10 cells were infected with L. monocytogenes (Lm) at MOI=10. (A-B) Mean percentage (analyzed by Mann-Whitney) of Lm SD2000 inoculum that was gentamicin-resistant 1 hr post-infection (hpi) in (A) SVEC4–10 cells or (B) Caco-2 cells. (C) Intracellular growth assay using stationary phase Lm SD2000. For panels A and C, mean values (±SEM) for triplicate samples from one of two experiments is shown. For panel B, mean values (±SEM) for quadruplet samples from one experiments is shown. (D) Representative images for differential “in/out” staining of cells infected with stationary phase Lm SD2710 (constitutive GFP), fixed at 4 hpi, and stained with DAPI (nucleus/blue), and anti-Listeria antibody (Lm/red). Scale bar, 5 μm. Dashed line indicates the outline of infected cell from the brightfield image. (E) Stacked bar indicates the percentage of Lm-infected cells (n=300) with only intracellular bacteria (IC), both intracellular and extracellular (IC+ EC), or only extracellular bacteria (EC). (F) Violin plot indicates the number of intracellular Lm observed per cell (n=300). For panels C, D and E data from one of two independent experiments are shown. (G) Representative image for <t>phalloidin</t> staining of SVEC4–10 cells infected with Lm SD2710 at 4 hpi; white arrows indicate Lm associated with actin; yellow arrowhead indicates Lm not associated with actin. Scale bar, 10 μm. Two independent experiments (n=100 cells analyzed in each) were performed; in Exp. 1, 72% of Lm were associated with actin and in Exp. 2 80% were. (H) Representative images from one of three independent plaque assays using SVEC4–10 cells or L2 fibroblasts infected with Lm SD2000 and visualized 4 dpi.
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SVEC4–10 cells were infected with L. monocytogenes (Lm) at MOI=10. (A-B) Mean percentage (analyzed by Mann-Whitney) of Lm SD2000 inoculum that was gentamicin-resistant 1 hr post-infection (hpi) in (A) SVEC4–10 cells or (B) Caco-2 cells. (C) Intracellular growth assay using stationary phase Lm SD2000. For panels A and C, mean values (±SEM) for triplicate samples from one of two experiments is shown. For panel B, mean values (±SEM) for quadruplet samples from one experiments is shown. (D) Representative images for differential “in/out” staining of cells infected with stationary phase Lm SD2710 (constitutive GFP), fixed at 4 hpi, and stained with DAPI (nucleus/blue), and anti-Listeria antibody (Lm/red). Scale bar, 5 μm. Dashed line indicates the outline of infected cell from the brightfield image. (E) Stacked bar indicates the percentage of Lm-infected cells (n=300) with only intracellular bacteria (IC), both intracellular and extracellular (IC+ EC), or only extracellular bacteria (EC). (F) Violin plot indicates the number of intracellular Lm observed per cell (n=300). For panels C, D and E data from one of two independent experiments are shown. (G) Representative image for <t>phalloidin</t> staining of SVEC4–10 cells infected with Lm SD2710 at 4 hpi; white arrows indicate Lm associated with actin; yellow arrowhead indicates Lm not associated with actin. Scale bar, 10 μm. Two independent experiments (n=100 cells analyzed in each) were performed; in Exp. 1, 72% of Lm were associated with actin and in Exp. 2 80% were. (H) Representative images from one of three independent plaque assays using SVEC4–10 cells or L2 fibroblasts infected with Lm SD2000 and visualized 4 dpi.
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Image Search Results


Primary and secondary antibodies used in this study

Journal: Neural Regeneration Research

Article Title: Prolonged intermittent theta burst stimulation restores the balance between A 2A R- and A 1 R-mediated adenosine signaling in the 6-hydroxidopamine model of Parkinson’s disease

doi: 10.4103/NRR.NRR-D-23-01542

Figure Lengend Snippet: Primary and secondary antibodies used in this study

Article Snippet: Rabbit anti-goat IgG, HRP-conjugated , Rabbit, polyclonal , 1:10000 WB , R and D Systems, Minneapolis, MN, USA , HAF017 , AB_562588.

Techniques: Western Blot, Immunohistochemistry

SVEC4–10 cells were infected with L. monocytogenes (Lm) at MOI=10. (A-B) Mean percentage (analyzed by Mann-Whitney) of Lm SD2000 inoculum that was gentamicin-resistant 1 hr post-infection (hpi) in (A) SVEC4–10 cells or (B) Caco-2 cells. (C) Intracellular growth assay using stationary phase Lm SD2000. For panels A and C, mean values (±SEM) for triplicate samples from one of two experiments is shown. For panel B, mean values (±SEM) for quadruplet samples from one experiments is shown. (D) Representative images for differential “in/out” staining of cells infected with stationary phase Lm SD2710 (constitutive GFP), fixed at 4 hpi, and stained with DAPI (nucleus/blue), and anti-Listeria antibody (Lm/red). Scale bar, 5 μm. Dashed line indicates the outline of infected cell from the brightfield image. (E) Stacked bar indicates the percentage of Lm-infected cells (n=300) with only intracellular bacteria (IC), both intracellular and extracellular (IC+ EC), or only extracellular bacteria (EC). (F) Violin plot indicates the number of intracellular Lm observed per cell (n=300). For panels C, D and E data from one of two independent experiments are shown. (G) Representative image for phalloidin staining of SVEC4–10 cells infected with Lm SD2710 at 4 hpi; white arrows indicate Lm associated with actin; yellow arrowhead indicates Lm not associated with actin. Scale bar, 10 μm. Two independent experiments (n=100 cells analyzed in each) were performed; in Exp. 1, 72% of Lm were associated with actin and in Exp. 2 80% were. (H) Representative images from one of three independent plaque assays using SVEC4–10 cells or L2 fibroblasts infected with Lm SD2000 and visualized 4 dpi.

Journal: Journal of Leukocyte Biology

Article Title: Lymph node stromal cells vary in susceptibility to infection but can support the intracellular growth of Listeria monocytogenes

doi: 10.1093/jleuko/qiae040

Figure Lengend Snippet: SVEC4–10 cells were infected with L. monocytogenes (Lm) at MOI=10. (A-B) Mean percentage (analyzed by Mann-Whitney) of Lm SD2000 inoculum that was gentamicin-resistant 1 hr post-infection (hpi) in (A) SVEC4–10 cells or (B) Caco-2 cells. (C) Intracellular growth assay using stationary phase Lm SD2000. For panels A and C, mean values (±SEM) for triplicate samples from one of two experiments is shown. For panel B, mean values (±SEM) for quadruplet samples from one experiments is shown. (D) Representative images for differential “in/out” staining of cells infected with stationary phase Lm SD2710 (constitutive GFP), fixed at 4 hpi, and stained with DAPI (nucleus/blue), and anti-Listeria antibody (Lm/red). Scale bar, 5 μm. Dashed line indicates the outline of infected cell from the brightfield image. (E) Stacked bar indicates the percentage of Lm-infected cells (n=300) with only intracellular bacteria (IC), both intracellular and extracellular (IC+ EC), or only extracellular bacteria (EC). (F) Violin plot indicates the number of intracellular Lm observed per cell (n=300). For panels C, D and E data from one of two independent experiments are shown. (G) Representative image for phalloidin staining of SVEC4–10 cells infected with Lm SD2710 at 4 hpi; white arrows indicate Lm associated with actin; yellow arrowhead indicates Lm not associated with actin. Scale bar, 10 μm. Two independent experiments (n=100 cells analyzed in each) were performed; in Exp. 1, 72% of Lm were associated with actin and in Exp. 2 80% were. (H) Representative images from one of three independent plaque assays using SVEC4–10 cells or L2 fibroblasts infected with Lm SD2000 and visualized 4 dpi.

Article Snippet: Permeabilized cells were incubated with goat anti-rabbit IgG-Texas Red-X phalloidin (ThermoFisher) diluted 1:100 in TBS+BSA for 30 min at room temperature.

Techniques: Infection, MANN-WHITNEY, Growth Assay, Staining, Bacteria

LNSC were sort-purified from the MLN and PLN of uninfected BALBc/ByJ mice and infected with Lm at an MOI of 10. (A) Gentamicin protection assay for cells infected with Lm SD2000; pooled data from eight separate experiments (each designated by a different symbol type) were analyzed by ANOVA with Tukeys multiple comparison test. In each experiment, total cells sorted from three mice were used at two time points. (B) Representative images for differential ”in/out” staining of sort-purified LNSC infected with Lm SD2710 (GFP+), fixed at 8 hpi and stained with DAPI (nuclei; blue), and anti-Lm antibody (red); scale bar, 5 μm. (C) Symbols indicate the number of intracellular Lm observed in a single infected cell; horizontal lines indicate median values for n=100 cells. For panels B and C, data from one of two independent experiments are shown. (D) Representative images for phalloidin staining of cells infected with Lm SD2710. White arrows indicate actin tails associated with Lm; yellow arrowheads indicate Lm not associated with actin. Scale bar, 5 μm. (E) Mean percent (±SEM) of intracellular Lm associated with actin. Each symbol represents results from a single experiment. (F) IFNβ present in supernatants of uninfected (U) and Lm SD2000-infected (Lm) cells (3 × 104 cells/well) at 16 hours was measured by multiplex immunoassay; symbols indicate mean values (+/− SEM) for duplicate samples from three separate experiments and were analyzed by one-way ANOVA. (G) Fold change of cytokine responses measured by multiplex immunoassay in Lm-infected cells relative to uninfected cells. Dashed lines indicate limits of detection.

Journal: Journal of Leukocyte Biology

Article Title: Lymph node stromal cells vary in susceptibility to infection but can support the intracellular growth of Listeria monocytogenes

doi: 10.1093/jleuko/qiae040

Figure Lengend Snippet: LNSC were sort-purified from the MLN and PLN of uninfected BALBc/ByJ mice and infected with Lm at an MOI of 10. (A) Gentamicin protection assay for cells infected with Lm SD2000; pooled data from eight separate experiments (each designated by a different symbol type) were analyzed by ANOVA with Tukeys multiple comparison test. In each experiment, total cells sorted from three mice were used at two time points. (B) Representative images for differential ”in/out” staining of sort-purified LNSC infected with Lm SD2710 (GFP+), fixed at 8 hpi and stained with DAPI (nuclei; blue), and anti-Lm antibody (red); scale bar, 5 μm. (C) Symbols indicate the number of intracellular Lm observed in a single infected cell; horizontal lines indicate median values for n=100 cells. For panels B and C, data from one of two independent experiments are shown. (D) Representative images for phalloidin staining of cells infected with Lm SD2710. White arrows indicate actin tails associated with Lm; yellow arrowheads indicate Lm not associated with actin. Scale bar, 5 μm. (E) Mean percent (±SEM) of intracellular Lm associated with actin. Each symbol represents results from a single experiment. (F) IFNβ present in supernatants of uninfected (U) and Lm SD2000-infected (Lm) cells (3 × 104 cells/well) at 16 hours was measured by multiplex immunoassay; symbols indicate mean values (+/− SEM) for duplicate samples from three separate experiments and were analyzed by one-way ANOVA. (G) Fold change of cytokine responses measured by multiplex immunoassay in Lm-infected cells relative to uninfected cells. Dashed lines indicate limits of detection.

Article Snippet: Permeabilized cells were incubated with goat anti-rabbit IgG-Texas Red-X phalloidin (ThermoFisher) diluted 1:100 in TBS+BSA for 30 min at room temperature.

Techniques: Purification, Infection, Comparison, Staining, Multiplex Assay

Antibodies used in this study

Journal: Neural Regeneration Research

Article Title: NOX4 exacerbates Parkinson’s disease pathology by promoting neuronal ferroptosis and neuroinflammation

doi: 10.4103/NRR.NRR-D-23-01265

Figure Lengend Snippet: Antibodies used in this study

Article Snippet: Goat anti rabbit IgG-HRP , goat anti-rabbit , Huabio, Hangzhou, China , AB_2819166/HA1001 , WB (1:5000).

Techniques: