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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Proteintech antibax antibody
Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 <t>polyclonal</t> antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
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Image Search Results


Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 polyclonal antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.

Journal: FEMS Immunology & Medical Microbiology

Article Title: Chlamydia (Chlamydophila) pneumoniae-induced cell death in human coronary artery endothelial cells is caspase-independent and accompanied by subcellular translocations of Bax and apoptosis-inducing factor

doi: 10.1111/j.1574-695x.2006.00083.x

Figure Lengend Snippet: Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 polyclonal antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.

Article Snippet: Cells were washed twice in phosphate-buffered saline (PBS) and fixed in 4% paraformaldehyde in PBS for 15 min. After washing, cells were incubated for 30 min in N-20 antiBax rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) at 1 : 50 dilution in permeabilization buffer (bovine serum albumin (BSA) 1 g L 1, 0.05% saponin in PBS), washed twice in PBS-BSA, blocked in 4% normal goat serum for 30 min, washed in PBS-BSA and visualized by incubation for 30 min with a 1 : 100 dilution of Alexa Fluor 568 F(ab0)2 goat antirabbit IgG antibody (Molecular Probes, Eugene, OR).

Techniques: Translocation Assay, Infection, Incubation, Microscopy, Standard Deviation

Fig. 5. Subcellular translocation of apoptosis-inducing factor (AIF) dur- ing Chlamydia pneumoniae infection of human coronary artery endo- thelial cells. (a) Cells were infected with Chlamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-19 polyclonal antibody towards AIF and secondary antibody. Cells with nuclear fluorescence were enumerated by fluorescence microscopy. Bars represent mean standard deviation of nine to 11 experiments. P o 0.05. (b) Subcellular localization of AIF in uninfected cells showing cytosolic fluorescence. (c) Subcellular localization of AIF in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing nuclear fluorescence.

Journal: FEMS Immunology & Medical Microbiology

Article Title: Chlamydia (Chlamydophila) pneumoniae-induced cell death in human coronary artery endothelial cells is caspase-independent and accompanied by subcellular translocations of Bax and apoptosis-inducing factor

doi: 10.1111/j.1574-695x.2006.00083.x

Figure Lengend Snippet: Fig. 5. Subcellular translocation of apoptosis-inducing factor (AIF) dur- ing Chlamydia pneumoniae infection of human coronary artery endo- thelial cells. (a) Cells were infected with Chlamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-19 polyclonal antibody towards AIF and secondary antibody. Cells with nuclear fluorescence were enumerated by fluorescence microscopy. Bars represent mean standard deviation of nine to 11 experiments. P o 0.05. (b) Subcellular localization of AIF in uninfected cells showing cytosolic fluorescence. (c) Subcellular localization of AIF in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing nuclear fluorescence.

Article Snippet: Cells were washed twice in phosphate-buffered saline (PBS) and fixed in 4% paraformaldehyde in PBS for 15 min. After washing, cells were incubated for 30 min in N-20 antiBax rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) at 1 : 50 dilution in permeabilization buffer (bovine serum albumin (BSA) 1 g L 1, 0.05% saponin in PBS), washed twice in PBS-BSA, blocked in 4% normal goat serum for 30 min, washed in PBS-BSA and visualized by incubation for 30 min with a 1 : 100 dilution of Alexa Fluor 568 F(ab0)2 goat antirabbit IgG antibody (Molecular Probes, Eugene, OR).

Techniques: Translocation Assay, Infection, Incubation, Microscopy, Standard Deviation