fix

wiki/experiments/section-9.html

@@ -72,7 +72,7 @@
         <li>
           Create the reaction system by adding the following reagents in their assigned portions into a microtube.
 
-          <table class="rw-100 m-t-1">
+          <table class="rw-75 mx-auto text-center m-t-1 table-head-bg-blue">
             <tbody>
             <tr>
               <th>Reagent</th>
@@ -94,16 +94,6 @@
               <td>2μl</td>
               <td>0.8μM</td>
             </tr>
-            <tr>
-              <td>Loop F (10μM)</td>
-              <td>1μl</td>
-              <td>0.4μM</td>
-            </tr>
-            <tr>
-              <td>Loop B (10μM)</td>
-              <td>1μl</td>
-              <td>0.4μM</td>
-            </tr>
             <tr>
               <td>F3 (10μM)</td>
               <td>0.5μl</td>
@@ -116,7 +106,7 @@
             </tr>
             <tr>
               <td>Template DNA</td>
-              <td>25-100 ng</td>
+              <td>1.5μl</td>
               <td>1-4 ng/μl</td>
             </tr>
             <tr>
@@ -126,20 +116,41 @@
             </tr>
             <tr>
               <td>Sterilized ddH2O</td>
-              <td>Up to 25μl</td>
+              <td>5.5μl</td>
               <td>-</td>
             </tr>
             </tbody>
           </table>
         </li>
         <li>
-          Place the microtube into a 65C water bath and heat it for 30-60 minutes.
+          Place the microtube into a 65℃ water bath and heat it for 30-60 minutes.
         </li>
         <li>
-          Place the tube in a gradient thermo cycler and heat at 80C for 10 minutes to denature all DNA polymerase
+          Place the tube in a gradient thermo cycler and heat at 80℃ for 10 minutes to denature all DNA polymerase.
         </li>
-      </ol>
+        <li>
+          Test resulting DNA using gel electrophoresis:
 
+          <ol type="a">
+            <li>
+              Prepare 1% gel electrophoresis by preparing the gel
+            </li>
+            <li>
+              Pipette 3-5μl of LAMP resultant using a pipette and run gel electrophoresis at 180V for 10 minutes.
+            </li>
+            <li>
+              Agarose electrophoresis was used for detection. Take 3-5μl amplification products, prepare 1% agar gel for
+              electrophoresis detection, and lamp characteristic maps composed of different size bands can be seen.
+            </li>
+          </ol>
+        </li>
+      </ol>
+      <div class="imager">
+        <img class="rw-100" src="https://static.igem.wiki/teams/4304/wiki/experiments/t-ykpao-experiments-01.jpg" alt="">
+      </div>
+      <div class="imager">
+        <img class="rw-100" src="https://static.igem.wiki/teams/4304/wiki/experiments/t-ykpao-experiments-02.jpg" alt="">
+      </div>
     </div>
   </div>
 </section>
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