Team:Warsaw/Calendar-Main/3 June 2008

From 2008.igem.org

(Difference between revisions)
Line 5: Line 5:
<h3>Preparation of T7 constructs<br>Piotr</h3>
<h3>Preparation of T7 constructs<br>Piotr</h3>
-
<ul>
+
<ol>
<li>DNA (PCR products from previous day) gel electrophoresis and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">isolation</a> of DNA from proper bands. </li>
<li>DNA (PCR products from previous day) gel electrophoresis and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">isolation</a> of DNA from proper bands. </li>
Line 13: Line 13:
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_purification_after_enzymatic_reaction">Clean-up</a> of reaction products.</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_purification_after_enzymatic_reaction">Clean-up</a> of reaction products.</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of p.4 products (pMPM-T5 + AID transcription fusion with AID-T7 RNA-polymerase translation fusion).</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of p.4 products (pMPM-T5 + AID transcription fusion with AID-T7 RNA-polymerase translation fusion).</li>
-
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#electrotransform">Transformation</a> of <i>E.coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> with ligation product.</li>
+
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#chemotransform">Transformation</a> of <i>E.coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> with ligation product.</li>
<li>Plating transformants on LB+tetracycline.</li>
<li>Plating transformants on LB+tetracycline.</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">Digest</a> of pMPM-T5 + transcription fusion with EcoRHI and HindIII.</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">Digest</a> of pMPM-T5 + transcription fusion with EcoRHI and HindIII.</li>
Line 20: Line 20:
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Isolation of DNA from proper band.</a></li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Isolation of DNA from proper band.</a></li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of product p.11 (pMPM-T5 + T7 RNA-polymerase).</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of product p.11 (pMPM-T5 + T7 RNA-polymerase).</li>
-
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#electrotransform">Transformation</a> of <i>E.coli</i> TOP10 with ligation product.</li>
+
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#chemotransform">Transformation</a> of <i>E.coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> with ligation product.</li>
<li>Plating transformants on LB + tetracycline.</li>
<li>Plating transformants on LB + tetracycline.</li>
-
</ul>
+
</ol>
<html>
<html>
<img src="https://static.igem.org/mediawiki/2008/a/a4/UW_AAT.jpg" width="500"/>
<img src="https://static.igem.org/mediawiki/2008/a/a4/UW_AAT.jpg" width="500"/>

Revision as of 23:24, 4 October 2008

Gallery Bricks Notebook Team Project Home


Previous day
return to main notebook page
Previous entry
next notebook entry

 


Preparation of T7 constructs
Piotr

  1. DNA (PCR products from previous day) gel electrophoresis and isolation of DNA from proper bands.
  2. Digest of DNA with HindIII and SalI (2x Tango buffer).
  3. Digest of pMPM-T5 + AID with HindIII and SalI.
  4. Clean-up of reaction products.
  5. Ligation of p.4 products (pMPM-T5 + AID transcription fusion with AID-T7 RNA-polymerase translation fusion).
  6. Transformation of E.coli TOP10 with ligation product.
  7. Plating transformants on LB+tetracycline.
  8. Digest of pMPM-T5 + transcription fusion with EcoRHI and HindIII.
  9. Use of T4 polymerase for blunting.
  10. DNA gel electrophoresis.
  11. Isolation of DNA from proper band.
  12. Ligation of product p.11 (pMPM-T5 + T7 RNA-polymerase).
  13. Transformation of E.coli TOP10 with ligation product.
  14. Plating transformants on LB + tetracycline.