Team:USTC CHINA/Notebook/Protocols/Plasmid mini-prep

From 2013.igem.org

(Difference between revisions)
 
(One intermediate revision not shown)
Line 9: Line 9:
<div id="igemlogo"><a href="https://2013.igem.org/Main_Page" target="_blank"><img src="https://static.igem.org/mediawiki/2013/2/26/2013ustcigem_IGEM_basic_Logo.png" alt="igem home page" width="50" height="40" /></a></div>
<div id="igemlogo"><a href="https://2013.igem.org/Main_Page" target="_blank"><img src="https://static.igem.org/mediawiki/2013/2/26/2013ustcigem_IGEM_basic_Logo.png" alt="igem home page" width="50" height="40" /></a></div>
-
    <ul id="nav">
+
<ul id="nav">
         <li><a href="https://2013.igem.org/Team:USTC_CHINA">Home</a></li>
         <li><a href="https://2013.igem.org/Team:USTC_CHINA">Home</a></li>
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/Overview">Project</a>
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/Overview">Project</a>
Line 16: Line 16:
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/ProjectDetails">Project Details</a></li>
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/ProjectDetails">Project Details</a></li>
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/Results">Results</a></li>
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/Results">Results</a></li>
-
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Project/Parts">Parts</a></li>
+
                 <li><a href="https://2013.igem.org/Team:USTC_CHINA/Parts">Parts</a></li>
             </ul>
             </ul>
         </li>
         </li>
Line 27: Line 27:
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/">Modeling</a>
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/">Modeling</a>
               <ul class="subs">
               <ul class="subs">
-
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/ReporterSystem">Reporter System</a></li>
+
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/KillSwitch">Kill Switch</a></li>
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/B.SubtilisCulture">B.Subtilis Culture</a></li>
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/B.SubtilisCulture">B.Subtilis Culture</a></li>
-
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/MiceModeling">Mice Modeling</a></li>
+
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Modeling/DesignsofImmuneExperiments">Designs of Immune Experiments</a></li>
               </ul>
               </ul>
         </li>
         </li>
Line 38: Line 38:
               </ul>
               </ul>
         </li>
         </li>
-
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/team2">Team</a>
+
         <li><a href="https://2013.igem.org/Team:USTC_CHINA/Team">Team</a>
               <ul class="subs">
               <ul class="subs">
-
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/team2">Members</a></li>
+
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Team">Members</a></li>
                   <li><a href="https://igem.org/Team.cgi?year=2013&team_name=USTC_CHINA">Profile</a></li>
                   <li><a href="https://igem.org/Team.cgi?year=2013&team_name=USTC_CHINA">Profile</a></li>
-
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Team/Attribution">Attribution</a></li>
+
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Attributions">Attributions</a></li>
-
                   <li><a href="https://2013.igem.org/Team:USTC_CHINA/Team/JudgingForm">Judging Form</a></li>
+
                   <li><a href="https://igem.org/2013_Judging_Form?id=1074#iGEM_Medals">Achievements</a></li>
               </ul>
               </ul>
         </li>
         </li>
Line 74: Line 74:
<div style="width:580px;height:655px;border-radius:1em 1em 1em 1em;background:#ffffff;border:1px solid rgb(68,68,68);padding:5px;">
<div style="width:580px;height:655px;border-radius:1em 1em 1em 1em;background:#ffffff;border:1px solid rgb(68,68,68);padding:5px;">
<div style="float:left;width:265px;">
<div style="float:left;width:265px;">
-
<img src="https://static.igem.org/mediawiki/2013/3/30/Plasmid_mini-prep1.png" width="265" height="443" />  </div>
+
<img src="https://static.igem.org/mediawiki/2013/3/3d/Plasmid_mini-prep11_%E5%89%AF%E6%9C%AC.png" width="265" height="443" />  </div>
<div style="float:left;width:199px;">
<div style="float:left;width:199px;">
-
<img src="https://static.igem.org/mediawiki/2013/1/18/Plasmid_mini-prep2.png" width="199" height="291" />  </div>
+
<img src="https://static.igem.org/mediawiki/2013/3/3c/Plasmid_mini-prep21_%E5%89%AF%E6%9C%AC.png" width="199" height="291" />  </div>
<div class="clear"></div>
<div class="clear"></div>
<div style="float:left;width:231px;">
<div style="float:left;width:231px;">
-
<img src="https://static.igem.org/mediawiki/2013/7/77/Plasmid_mini-prep3.png" width="231" height="208" />  </div>
+
<img src="https://static.igem.org/mediawiki/2013/7/7d/Prep31_%E5%89%AF%E6%9C%AC.png" width="231" height="208" />  </div>
</div>
</div>
</div>
</div>

Latest revision as of 16:50, 27 September 2013

Plasmid mini-prep

Performed with Shanghai Sangon Plasmid miniprep kit.
1. Preparation
1) Make sure the RNase A has been added into Buffer P1;
2) Make sure the ethanol has been added into Wash Solution;
3) Make sure there is no deposit in Buffer P2 and P3;
2. Collect the deposit of bacteria from 1.5ml~5ml bacteria liquid (centrifuge at 8,000×g for 2 min).
3. Add 250μl Buffer P1 into the deposit and suspend it thoroughly.
4. Add 250μl Buffer P2, mix gently and keep standing in room temperature for 2~4min.
5. Add 350μl Buffer P3 and mix gently for 5~10 times.
6. Precipitate the bacteria fragments (centrifuge at 12,000×g for 5~10 min) and extract the supernatant (centrifuge at 8,000×g for 30s).
7. Add 500 μl Buffer DW1, centrifuge at 9,000×g for 30s
8. Add 500 μl Wash Solution, centrifuge at 9,000×g for 30s. Repeat this process for one more time. Centrifuge the empty bottle at 9,000×g for 60s.
9. Add 50~100μl Elution Buffer and collect the plasmid.