patch 2

wiki/pages/experiments.html

@@ -351,7 +351,7 @@
     <li style="list-style:disc;">Transfer the GeneJET column to a 1.5 mL microcentrifuge tube</li>
     <li style="list-style:disc;">Add 50 μL of the Elution Buffer and incubate at room temperature for 2 minutes</li>
     <li style="list-style:disc;">Centrifuge for 2 minutes and discard the column. Ensure that the flowthrough is stored safelyh</li>
-  <ul>
+  </ul>
   <p>After nanodropping the plasmids from the miniprep, we decided to only use A11, C11, and E11 since, although G11 had high concentration, they had the highest purity (high 260/280 ratio).</p>
 
   <h3>PCR Purification Column</h3>