Team:Hannover/Results/GFP

From 2014.igem.org

(Difference between revisions)
(Created page with "{{Template:Team:Hannover/igem.css}} {{Template:Team:Hannover/main.css}} {{Template:Team:Hannover/main.tmpl}} {{Template:Team:Hannover/newmenu.tmpl}} <html> <body> <h1>Results / G...")
Line 6: Line 6:
<body>
<body>
<h1>Results / GFP Photos</h1><p class="text">To avoid cytotoxic effects on the plant caused by the heavy metals we decided to place T4MBP to the cell exterior. With a secretion signal (Expa4) the T4MBP is directed to the extracellular space. The protein is tethered to the cell surface by using a cellulose binding domain (CBD). Via the cellulose binding domain the protein is attached to the cell wall.</p>
<h1>Results / GFP Photos</h1><p class="text">To avoid cytotoxic effects on the plant caused by the heavy metals we decided to place T4MBP to the cell exterior. With a secretion signal (Expa4) the T4MBP is directed to the extracellular space. The protein is tethered to the cell surface by using a cellulose binding domain (CBD). Via the cellulose binding domain the protein is attached to the cell wall.</p>
-
<h2>Labwork</h2><p class="text"><ul><li>CBD fused with mGFP using<a href="" target="_blank"> our EMP protocol</a></li><ol><li>we used pEarleyGate with the sequenz of mGFP5 as a template to generate our megaprimer</li><li>we used our GenArt Vector (with the sequenz of a 5'UTR and the EXPA4 signal peptide followed by the T4MBP-construct, a FLAG epitope tag and the CBD) as the target plasmid</li></ol><li>.....</li></ul></p>
+
<h2>Labwork</h2><p class="text"><ul><li>CBD fused with mGFP using<a href="" target="_blank"> our EMP protocol</a></li><ol><li>we used pEarleyGate with the sequenz of mGFP5 as a template to generate our megaprimer</li><li>we used our GenArt Vector (with the sequenz of a 5'UTR and the EXPA4 signal peptide followed by the T4MBP, a tag and the CBD) as the target plasmid</li></ol><li>.....</li></ul></p>
<h2>Results</h2>
<h2>Results</h2>
<center><table><tr><td><a href="https://static.igem.org/mediawiki/2014/6/6b/Hannover_20141004_Figure_confocal_replicate1.png" data-lightbox="galery3" data-title="Fig. 3: confocal detection of fluorescence from transformed plant cells (replicate 1)
<center><table><tr><td><a href="https://static.igem.org/mediawiki/2014/6/6b/Hannover_20141004_Figure_confocal_replicate1.png" data-lightbox="galery3" data-title="Fig. 3: confocal detection of fluorescence from transformed plant cells (replicate 1)

Revision as of 12:22, 12 October 2014

Results / GFP Photos

To avoid cytotoxic effects on the plant caused by the heavy metals we decided to place T4MBP to the cell exterior. With a secretion signal (Expa4) the T4MBP is directed to the extracellular space. The protein is tethered to the cell surface by using a cellulose binding domain (CBD). Via the cellulose binding domain the protein is attached to the cell wall.

Labwork

  • CBD fused with mGFP using our EMP protocol
    1. we used pEarleyGate with the sequenz of mGFP5 as a template to generate our megaprimer
    2. we used our GenArt Vector (with the sequenz of a 5'UTR and the EXPA4 signal peptide followed by the T4MBP, a tag and the CBD) as the target plasmid
  • .....

Results

Fig. 3: confocal detection of fluorescence from transformed plant cells (replicate 1) Transformed cells of Nicotiana tabacum were analyzed via confocal microscopy. Colum A-I: red channel, shows chlorophyll’s autofluorescence which shows the chloroplasts. Colum B-J: green channel showing GFP. Colum C-K: red and green channel merged. Colum D-L: pseudo transmission detection. Lane A-D shows a transformed cell with raw GFP. Lane E-H shows a plasmamembranemarker (Nelson et al. 2007). Lane I-L shows the detection of the analyzed construct: Expa4-GFP-CBD.