"
Team:TU Darmstadt/Notebook/Methods/Agarose gel electrophoresis
From 2014.igem.org
(Difference between revisions)
(Created page with "{{:Team:TU_Darmstadt/Template}} <html> <div id="contentWrap" class="container_24"> <div id="breadcrumbs" class="grid_24"> <p>Sie sind hier: <a href="index.php...") |
|||
| Line 15: | Line 15: | ||
</div> | </div> | ||
| - | <div id=" | + | <div id="wikicontent" class="grid_19"> |
<!--TYPO3SEARCH_begin--><div id="c83" class="csc-default"><div class="csc-header csc-header-n1"><h1 class="csc-firstHeader">Agarose gel electrophoresis</h1></div><div><p><b>Short explanation:</b></p></div><div><p>Agarose gel electrophoresis is the most common used method to separate nucleic acids. Due to their negativ charge DNA and RNA molecules can be moved through an agarose gel by an electric field (electrophoresis). Longer molecules move slower through the agarose matrix while short move faster and migrate further.</p></div><div></div><div><p><b>Procedure:</b></p></div><div><p>In common we used 1% agarose gel.</p></div><div><p>1. The hot and liquid agarose gel is mixed with 4 µl NANCY for 50 ml of agarosegel (Shake in a bottle)</p></div><div><p>2. Fill everything in a chamber and let it cool down (do not forget the well combs)</p></div><div><p>3. Take 1xTAE-Buffer for the run</p></div><div><p>4. In the first ten minutes run the gel with 80 V and afterwards select 120V</p></div></div><!--TYPO3SEARCH_end--> | <!--TYPO3SEARCH_begin--><div id="c83" class="csc-default"><div class="csc-header csc-header-n1"><h1 class="csc-firstHeader">Agarose gel electrophoresis</h1></div><div><p><b>Short explanation:</b></p></div><div><p>Agarose gel electrophoresis is the most common used method to separate nucleic acids. Due to their negativ charge DNA and RNA molecules can be moved through an agarose gel by an electric field (electrophoresis). Longer molecules move slower through the agarose matrix while short move faster and migrate further.</p></div><div></div><div><p><b>Procedure:</b></p></div><div><p>In common we used 1% agarose gel.</p></div><div><p>1. The hot and liquid agarose gel is mixed with 4 µl NANCY for 50 ml of agarosegel (Shake in a bottle)</p></div><div><p>2. Fill everything in a chamber and let it cool down (do not forget the well combs)</p></div><div><p>3. Take 1xTAE-Buffer for the run</p></div><div><p>4. In the first ten minutes run the gel with 80 V and afterwards select 120V</p></div></div><!--TYPO3SEARCH_end--> | ||
</div> | </div> | ||
Revision as of 19:21, 15 October 2014
Agarose gel electrophoresis
Short explanation:
Agarose gel electrophoresis is the most common used method to separate nucleic acids. Due to their negativ charge DNA and RNA molecules can be moved through an agarose gel by an electric field (electrophoresis). Longer molecules move slower through the agarose matrix while short move faster and migrate further.
Procedure:
In common we used 1% agarose gel.
1. The hot and liquid agarose gel is mixed with 4 µl NANCY for 50 ml of agarosegel (Shake in a bottle)
2. Fill everything in a chamber and let it cool down (do not forget the well combs)
3. Take 1xTAE-Buffer for the run
4. In the first ten minutes run the gel with 80 V and afterwards select 120V
