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( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using <t>Autodeblur</t> deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.
Autodeblur Deconvolution Software, supplied by Oxford Instruments, 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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Oxford Instruments autodeblur
( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using <t>Autodeblur</t> deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.
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( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using <t>Autodeblur</t> deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.
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Oxford Instruments autodeblur software
( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using <t>Autodeblur</t> deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.
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BioImaging Solutions Inc autodeblur
( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using <t>Autodeblur</t> deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.
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Image Search Results


( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using Autodeblur deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.

Journal: PLoS ONE

Article Title: The p21-Activated Kinase (PAK) Family Member PakD Is Required for Chemorepulsion and Proliferation Inhibition by Autocrine Signals in Dictyostelium discoideum

doi: 10.1371/journal.pone.0096633

Figure Lengend Snippet: ( A ) act15::PakD-GFP cells were grown in glass chamber slides overnight, then fixed and stained with DAPI (blue), imaged by fluorescence microscopy using a 100× objective, and processed using Autodeblur deconvolution software (Bitplane software, Zurich, Switzerland). PakD-GFP signal (green) is shown superimposed on a transmitted light image. Bar is 10 µm. ( B ) Live pakD – /act15::PakD-GFP cells grown as a colony in glass chamber slides were imaged by fluorescence microscopy. The imaged cell is moving upwards, as seen by time-lapse microscopy. The arrow indicates PakD-GFP at the rear of the cell. A single punctum structure is also visible. The cell border is shown with a dashed line. Bar is 10 µm. ( C ) PakD-GFP (green) does not colocalize with either the cell nucleus (blue) or with staining for an antibody against ddCP224 (Red), a marker for the centrosome. Bar is 5 µm.

Article Snippet: Z-stacks were then processed using Autodeblur deconvolution software (Bitplane software, Zurich, Switzerland).

Techniques: Staining, Fluorescence, Microscopy, Software, Time-lapse Microscopy, Marker