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Team:Paris Bettencourt/Electronic microscopy Dubey Ben-Yehuda
From 2011.igem.org
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| - | <h4>Figure 3. Intercellular Nanotubes Form between Neighboring B. subtilis Cells</h4> | + | <<center>h4>Figure 3. Intercellular Nanotubes Form between Neighboring B. subtilis Cells</h4></center> |
| + | <a href="https://2011.igem.org/File:BY_electronic.png"><img src="https://static.igem.org/mediawiki/2011/f/f6/BY_electronic.png" style="width:100%;"></a> | ||
| + | <p><b><center><u>Fig2:</u> Electronic microscopy from the Dubey-Ben-Yehuda article </center></b></p> | ||
<p>(A–D) PY79 cells were grown to midexponential phase, plated on LB agar, incubated for 6 hr at 37° C, and visualized by HR-SEM.</p> | <p>(A–D) PY79 cells were grown to midexponential phase, plated on LB agar, incubated for 6 hr at 37° C, and visualized by HR-SEM.</p> | ||
<p>(A) A typical field of B. subtilis cells (315,000). Green arrows indicate intercellular nanotubes connecting neighboring cells. The scale bar represents 5 mm. </p> | <p>(A) A typical field of B. subtilis cells (315,000). Green arrows indicate intercellular nanotubes connecting neighboring cells. The scale bar represents 5 mm. </p> | ||
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<p>(F) A magnification of the dashed square in (E). The arrow highlights the flow of GFP molecules within a tube. The scale bar represents 200 nm.</p> | <p>(F) A magnification of the dashed square in (E). The arrow highlights the flow of GFP molecules within a tube. The scale bar represents 200 nm.</p> | ||
<p>(G) An additional example of an immuno-EM section, showing the localization of a GFP molecule within a tube, as indicated by an arrow. The scale bar represents 200 nm.</p> | <p>(G) An additional example of an immuno-EM section, showing the localization of a GFP molecule within a tube, as indicated by an arrow. The scale bar represents 200 nm.</p> | ||
| - | <p><i>Extract from the Dubey and Ben-Yehuda article</i> </p> | + | <p><i>Extract from the Dubey and Ben-Yehuda article</i> <a href="http://bms.ucsf.edu/sites/ucsf-bms.ixm.ca/files/marjordan_06022011.pdf">[1]</a></p> |
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Revision as of 11:09, 7 September 2011
(A–D) PY79 cells were grown to midexponential phase, plated on LB agar, incubated for 6 hr at 37° C, and visualized by HR-SEM.
(A) A typical field of B. subtilis cells (315,000). Green arrows indicate intercellular nanotubes connecting neighboring cells. The scale bar represents 5 mm.
(B) A higher-magnification image (340,000) of the boxed region in (A). Membrane bulging is indicated by an asterisk (*). The scale bar represents 500 nm.
(C) An additional field of cells demonstrating the occurrence of a network of intercellular nanotubes (350,000). The scale bar represents 1 mm.
(D) A field of cells where a cluster of smaller nanotubes (highlighted by a dashed circle) as well as a more pronounced larger tube (indicated by an arrow) are apparent (3100,000). The scale bar represents 500 nm.
(E) An immuno-EM section of cocultured PY79 (gfp-) and SB444 (gfp+) cells, stained with anti-GFP and secondary gold-conjugated antibodies. Black dots indicate the expression and localization of GFP molecules. The scale bar represents 200 nm.
(F) A magnification of the dashed square in (E). The arrow highlights the flow of GFP molecules within a tube. The scale bar represents 200 nm.
(G) An additional example of an immuno-EM section, showing the localization of a GFP molecule within a tube, as indicated by an arrow. The scale bar represents 200 nm.
Extract from the Dubey and Ben-Yehuda article [1]
