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Nikon niselements microscope imaging software
Niselements Microscope Imaging Software, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon spinning disk confocal microscope
Spinning Disk Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon a1r confocal microscope
A1r Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon confocal fluorescence microscopy
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Confocal Fluorescence Microscopy, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss confocal microscope lsm 710
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Confocal Microscope Lsm 710, supplied by Carl Zeiss, 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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Nikon metrology nv
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Metrology Nv, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nikon inverted light microscope
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Inverted Light Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss fluorescence microscope axiovert 200m
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Fluorescence Microscope Axiovert 200m, supplied by Carl Zeiss, 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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Nikon ti2 high content microscope
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Ti2 High Content Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss lsm780 confocal microscope
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Lsm780 Confocal Microscope, supplied by Carl Zeiss, 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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Nikon bright field microscope
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Bright Field Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss lsm510 meta-uv confocal microscope
Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence <t>microscopy</t> shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.
Lsm510 Meta Uv Confocal Microscope, supplied by Carl Zeiss, 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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Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence microscopy shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.

Journal: Virology

Article Title: Porcine reproductive and respiratory syndrome virus induces HMGB1 secretion via activating PKC-delta to trigger inflammatory response.

doi: 10.1016/j.virol.2018.02.021

Figure Lengend Snippet: Fig. 7. PRRSV ORF2b and ORF5a products (E and pORF5a, respectively) are responsible for inducing HMGB1 secretion via activating PKCδ. A. Screening of PRRSV ORFs. HEK293 cells were transfected with individual GFP-ORF plasmids. The SUP and WCL were harvested 30 h after transfection for WB with antibodies against HMGB1, tubulin and GFP. Empty GFP vector (EV) was included as a control in the transient transfection. The expression of ORF2 and ORF3 were also confirmed by fluorescence microscopy shown in the right panel of GFP images. Bars in the images denote 50 µm. B. ORF2b and ORF5a products induce HMGB1 secretion in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of GFP- ORF2b or GFP-ORF5a plasmid, respectively. At 30 h after transfection, the SUP and WCL were harvested for WB. Relative levels of HMGB1 in SUP are shown as folds below the images in densitometry analysis. C. ORF2b and ORF5a products activate PKCδ. HEK293 cells were transfected with EV, ORF2b, ORF5 or ORF5a plasmid and 30 h later, harvested for WB with antibodies against PKCδ-S645, PKCδ, tubulin and GFP. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin. D. ORF2b and ORF5a products induce PKCδ activation in a dose-dependent manner. HEK293 cells were transfected with incremental amounts of ORF2b or ORF5a plasmid and 30 h after transfection, harvested for WB. Relative levels of PKCδ-S645 are shown as folds below the images after normalization with tubulin.

Article Snippet: Fluorescence signal was observed under confocal fluorescence microscopy (Nikon C2) and images were taken with NISElements version 4.0 (Nikon).

Techniques: Transfection, Plasmid Preparation, Control, Expressing, Microscopy, Activation Assay