Difference between revisions of "Team:EPF Lausanne/Notebook/Protocols"
| Line 160: | Line 160: | ||
</nav> | </nav> | ||
<div class="col-sm-9"> | <div class="col-sm-9"> | ||
| + | |||
| + | <!-- AGAROSE GEL --> | ||
<div id="agarosegel" class="well"> | <div id="agarosegel" class="well"> | ||
<h1>Agarose Gel</h1> | <h1>Agarose Gel</h1> | ||
| Line 181: | Line 183: | ||
<p> • Take a picture of the gel at the UV detector</p> | <p> • Take a picture of the gel at the UV detector</p> | ||
</div> | </div> | ||
| + | |||
| + | <!-- AMINO ACID SOLUTION --> | ||
<div id="aminoacidsolution" class="well"> | <div id="aminoacidsolution" class="well"> | ||
<h1>Amino acid solution</h1> | <h1>Amino acid solution</h1> | ||
| Line 190: | Line 194: | ||
<h2>Procedure</h2> | <h2>Procedure</h2> | ||
<table style=”width:100%”> | <table style=”width:100%”> | ||
| + | <thread> | ||
<tr> | <tr> | ||
<th>Stock concentration</th> | <th>Stock concentration</th> | ||
| Line 195: | Line 200: | ||
<th>Total quantity for 50 mL</th> | <th>Total quantity for 50 mL</th> | ||
</tr> | </tr> | ||
| + | </thread> | ||
| + | <tbody> | ||
<tr> | <tr> | ||
<th>100 mM Histidine-Hcl (209 g/mol)</th> | <th>100 mM Histidine-Hcl (209 g/mol)</th> | ||
| Line 215: | Line 222: | ||
<th> 0.1632 g</th> | <th> 0.1632 g</th> | ||
</tr> | </tr> | ||
| + | </tbody> | ||
</table> | </table> | ||
<p> • Filter and sterilize solutions</p> | <p> • Filter and sterilize solutions</p> | ||
<p> •Add 8 mL per liter of selective medium or spread 500 μL on a selective plate</p> | <p> •Add 8 mL per liter of selective medium or spread 500 μL on a selective plate</p> | ||
</div> | </div> | ||
| + | |||
| + | <!-- SECTION 3 --> | ||
<div id="section3" class="well"> | <div id="section3" class="well"> | ||
<h1>Section 3</h1> | <h1>Section 3</h1> | ||
<p>Try to scroll this section and look at the navigation list while scrolling!</p> | <p>Try to scroll this section and look at the navigation list while scrolling!</p> | ||
</div> | </div> | ||
| + | <!-- SECTION 4 --> | ||
<div id="section41" class="well"> | <div id="section41" class="well"> | ||
<h1>Section 4-1</h1> | <h1>Section 4-1</h1> | ||
Revision as of 13:21, 21 July 2015
Protocols
Agarose Gel
Materials
• 1X TAE
• Agarose
• Gel Red
• DNA samples
• 6X loading dye
• Nuclease free water
Procedure
Prepare 1.2% agarose gel for small fragments and 3% agarose gel for large fragments
• Mix 50 mL 1X TAE and 0.6 g (1.2%) or 1.5 g (3%) agarose
• Melt in microwave until agarose has melted (about 50 seconds)
• Add 1.3 μL (1.2%) or 1.5 μL (3%) Gel Red
• Pour solution into agarose gel mold with comb
• Let set for 20 minutes or until solid
• Place gel in 1X TAE and remove comb
• Load samples of 200 ng (or 2 μL) DNA mixed with 2 μL 6X loading dye and nuclease free water up to 12 μL
• Run gel at 100-120 Volts for 40-50 minutes (1.2%) or 80 Volts for 2 hours (3%)
• Take a picture of the gel at the UV detector
Amino acid solution
Materials
• Histidine-Hcl
• Uracil
• Leucine
• Tryptophan
Procedure
| Stock concentration | Final concentration | Total quantity for 50 mL |
|---|---|---|
| 100 mM Histidine-Hcl (209 g/mol) | 20.9 g/L | 0.418 g |
| 20 mM Uracil (112 g/mol) | 2.24 g/L | 0.0448 g |
| 100 mM Leucine (131 g/mol) | 13.1 g/L | 0.262 g |
| 40 mM Tryptophan (204 g/mol) | 8.16 g/L | 0.1632 g |
• Filter and sterilize solutions
•Add 8 mL per liter of selective medium or spread 500 μL on a selective plate
Section 3
Try to scroll this section and look at the navigation list while scrolling!
Section 4-1
Try to scroll this section and look at the navigation list while scrolling!
Section 4-2
Try to scroll this section and look at the navigation list while scrolling!