retiga exi camera Search Results


q imagine retiga exi 12-bit digital camera  (scanalytics inc)
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Q Imagine Retiga Exi 12 Bit Digital Camera, supplied by scanalytics 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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color ccd camera retiga exi cooled digital color model  (QImaging)
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Color Ccd Camera Retiga Exi Cooled Digital Color Model, supplied by QImaging, 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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digital camera q imaging retiga exi  (Image Systems Inc)
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Digital Camera Q Imaging Retiga Exi, supplied by Image Systems 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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fast firewire retiga exi chilled ccd camera  (QImaging)
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Fast Firewire Retiga Exi Chilled Ccd Camera, supplied by QImaging, 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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ccd camera retiga exi aqua  (QImaging)
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QImaging ccd camera retiga exi aqua
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Ccd Camera Retiga Exi Aqua, supplied by QImaging, 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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retiga exi non-cooled 12-bit digital ccd camera  (Empix Imaging)
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Empix Imaging retiga exi non-cooled 12-bit digital ccd camera
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Retiga Exi Non Cooled 12 Bit Digital Ccd Camera, supplied by Empix Imaging, 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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cooled mono 12-bit retiga exi fast charge-coupled device camera  (Quantitative Imaging Corporation)
90
Quantitative Imaging Corporation cooled mono 12-bit retiga exi fast charge-coupled device camera
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Cooled Mono 12 Bit Retiga Exi Fast Charge Coupled Device Camera, supplied by Quantitative Imaging Corporation, 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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camera qimaging retiga exi fast 13941 mono  (QImaging)
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QImaging camera qimaging retiga exi fast 13941 mono
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Camera Qimaging Retiga Exi Fast 13941 Mono, supplied by QImaging, 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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retiga exi fast camera  (QImaging)
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QImaging retiga exi fast camera
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Retiga Exi Fast Camera, supplied by QImaging, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/retiga+exi+camera/retiga+exi+fast+camera/ppr0361244-95-13-18
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digital camera demo retiga exi monochrome  (QImaging)
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QImaging digital camera demo retiga exi monochrome
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Digital Camera Demo Retiga Exi Monochrome, supplied by QImaging, 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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chilled charge-coupled device (ccd) camera retiga fast firewire exi  (QImaging)
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QImaging chilled charge-coupled device (ccd) camera retiga fast firewire exi
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Chilled Charge Coupled Device (Ccd) Camera Retiga Fast Firewire Exi, supplied by QImaging, 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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cooled ccd camera retiga exi  (scanalytics inc)
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scanalytics inc cooled ccd camera retiga exi
(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device <t>(CCD)</t> camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.
Cooled Ccd Camera Retiga Exi, supplied by scanalytics 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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Image Search Results


(A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device (CCD) camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.

Journal: PLoS Biology

Article Title: Viruses Roll the Dice: The Stochastic Behavior of Viral Genome Molecules Accelerates Viral Adaptation at the Cell and Tissue Levels

doi: 10.1371/journal.pbio.1002094

Figure Lengend Snippet: (A) The genome structure of wild-type ToMV and its derivatives used in the experiments. Rectangles indicate open reading frames (ORFs). MT, a methyltransferase-like domain; HEL, a helicase-like domain; POL, a polymerase-like domain of the replication proteins; MP, the cell-to-cell movement protein; and CP, the coat protein. Translation of the genomic RNA produces two replication proteins, 130K and 180K; 130K contains MT and HEL. The 180K is synthesized via the UAG stop codon read-through of 130K to express POL. FP indicates the fluorescent protein genes (YFP or CFP). TLPYFP-CP and TLPCFP-CP carry the YFP and CFP gene, respectively, between the MP and CP coding regions. The expression of the YFP or CFP genes is driven by a duplicated subgenomic promoter (sgp) for the CP. TLPYFP and TLPCFP lack the CP gene. The regions that correspond to the PPYP and P5′M probes, which were used for northern blotting and RNase protection assays, are indicated by bold lines. (B) An example of spatial separation of the two variants during cell-to-cell spread from a coinfected cell in a tobacco leaf. YFP and CFP fluorescence images were obtained separately 44 hours postinoculation (hpi) using a color charge-coupled device (CCD) camera. After converting the color of the CFP fluorescence image to magenta, the image was merged with the YFP fluorescence image without color conversion. The YFP images look green (rather than yellow) because of the transmission range of the emission filter. Coinfected cells were found at the central part of the infected region as white colored cells. (C) The stochastic occurrence of single infections by one of the two co-inoculated variants in protoplasts. Fluorescence images were obtained at 24 hpi and then processed as described above. White arrowheads indicate singly infected cells.

Article Snippet: Images were captured using a CCD camera Retiga EXi Aqua (QImaging, Surrey, British Columbia, Canada) and analyzed using Image-Pro Plus software (Media Cybernetics, Rockville, Maryland, US).

Techniques: Synthesized, Expressing, Northern Blot, Fluorescence, Transmission Assay, Infection