Team:UNIPV-Pavia/Methods Materials/Electrophoresis

From 2009.igem.org

(Difference between revisions)
(Electrophoresis)
(Electrophoresis)
 
(16 intermediate revisions not shown)
Line 1: Line 1:
 +
{{UNIPV-Pavia/StyleCss}}
<html>
<html>
Line 4: Line 5:
   <tr>
   <tr>
<td align="center">
<td align="center">
-
<img width="100%" height="180px" src="https://static.igem.org/mediawiki/2009/c/c2/UNIPV_title_MandM.jpg" ></img>
+
<img width="100%" height="180px" src="https://static.igem.org/mediawiki/2009/d/de/UNIPV_title_M%26M.jpg" ></img>
</td>
</td>
   </tr>
   </tr>
Line 21: Line 22:
     <font face="Pristina" size="50" ><b>Protocols</b></font>
     <font face="Pristina" size="50" ><b>Protocols</b></font>
     </td>
     </td>
 +
    <td width="50px"></td>
</html>
</html>
   </tr>
   </tr>
Line 46: Line 48:
*Take a picture of the gel, if needed (not when bands have to be cut!!!)
*Take a picture of the gel, if needed (not when bands have to be cut!!!)
<br><br><br><br><br><br><br><br>
<br><br><br><br><br><br><br><br>
-
<br></td><td align='center' valign='bottom' width='300px'>
+
<br></td><td align='center' valign='top' width='300px'>
-
<div align='center'>
+
 
<table border='1'>
<table border='1'>
 +
<tr bgcolor='yellow'><td>INGREDIENTS:
 +
</td></tr>
<tr><td>
<tr><td>
<font class='label'>
<font class='label'>
Line 54: Line 58:
'''Ethidium bromide'''<hr color='white' width='70%'>
'''Ethidium bromide'''<hr color='white' width='70%'>
'''Loading buffer 10x Blue Juice, Invitrogen'''<hr color='white' width='70%'>
'''Loading buffer 10x Blue Juice, Invitrogen'''<hr color='white' width='70%'>
-
'''TBE (Tris/Borate/EDTA buffer) 5x (final volume 1 liter)'''<hr color='white' width='70%'>
+
'''TBE (Tris/Borate/EDTA buffer) 5x (final volume 1 liter)'''
-
**'''54 gr Tris'''
+
*'''54 gr Tris'''
-
**'''27.5 gr Borate'''
+
*'''27.5 gr Borate'''<hr color='white' width='70%'>
'''20 ml EDTA 0.5 M (pH 8)'''<hr color='white' width='70%'>
'''20 ml EDTA 0.5 M (pH 8)'''<hr color='white' width='70%'>
'''Marker (1 kb DNA Ladder, Promega)'''<hr color='white' width='70%'>
'''Marker (1 kb DNA Ladder, Promega)'''<hr color='white' width='70%'>
Line 62: Line 66:
'''Electrophoresis apparatus'''<hr color='white' width='70%'>
'''Electrophoresis apparatus'''<hr color='white' width='70%'>
'''Transilluminator'''</font>
'''Transilluminator'''</font>
-
</td></tr></table></div><br><br><br><br>
+
</td></tr></table><br><br><br><br>
</td></tr></table>
</td></tr></table>

Latest revision as of 10:30, 21 October 2009

EthanolPVanimation.gif



Protocols


Electrophoresis

(estimated time: 2 hours)

  • Prepare agarose gel in 1x TBE buffer
  • Add ethidium bromide (using gloves and face mask for your safety):
    • 1 µl in the small size agarose gel (70 ml)
    • 2 µl in the middle size agarose gel (150 ml)
    • 4 µl in the big size agarose gel (250 ml)
  • Cast the gel, insert the well-forming comb and let it polymerize
  • Add the loading buffer to each sample
  • Load the samples and 8 µl of marker
  • Set to 70-100 volts and electrophorese for the required amount of time
  • Use UV-light to look at the bands
  • Take a picture of the gel, if needed (not when bands have to be cut!!!)










INGREDIENTS:

DNA samples
Ethidium bromide
Loading buffer 10x Blue Juice, Invitrogen

TBE (Tris/Borate/EDTA buffer) 5x (final volume 1 liter)

  • 54 gr Tris
  • 27.5 gr Borate
20 ml EDTA 0.5 M (pH 8)
Marker (1 kb DNA Ladder, Promega)
Face mask and gloves
Electrophoresis apparatus

Transilluminator





  • NOTE: when not specified, the marker has the following pattern:
Pv ladder.jpg