Team:USTC CHINA/Notebook/Protocols/Plasmid mini-prep
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- | <div id="breadcrumb"><a href="https://2013.igem.org/Team:USTC_CHINA">Home</a> > <a href="https://2013.igem.org/Team:USTC_CHINA/Notebook"> | + | <div id="breadcrumb"><a href="https://2013.igem.org/Team:USTC_CHINA">Home</a> > <a href="https://2013.igem.org/Team:USTC_CHINA/Notebook">Notebook</a> > <a href="https://2013.igem.org/Team:USTC_CHINA/Notebook/Protocols">Protocols</a> > <a href="https://2013.igem.org/Team:USTC_CHINA/Notebook/Protocols/Plasmid mini-prep">Plasmid mini-prep</a></div></div> |
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<div class="bassic-bar"> | <div class="bassic-bar"> | ||
- | <h1> | + | <h1>Plasmid mini-prep</h1> |
- | <p>Performed with Shanghai Sangon Plasmid miniprep kit. | + | <p><span>Performed with Shanghai Sangon Plasmid miniprep kit.</span></br> |
- | 1. Preparation | + | 1. Preparation</br> |
- | 1) Make sure the RNase A has been added into Buffer P1; | + | 1) Make sure the RNase A has been added into Buffer P1;</br> |
- | 2) Make sure the ethanol has been added into Wash Solution | + | 2) Make sure the ethanol has been added into Wash Solution;</br> |
- | 3) Make sure there is no deposit in Buffer P2 and P3 | + | 3) Make sure there is no deposit in Buffer P2 and P3;</br> |
- | 2. Collect the deposit of bacteria from 1.5ml~5ml bacteria liquid (centrifuge at 8,000×g for 2 min) | + | 2. Collect the deposit of bacteria from 1.5ml~5ml bacteria liquid (centrifuge at 8,000×g for 2 min).</br> |
- | + | 3. Add 250μl Buffer P1 into the deposit and suspend it thoroughly.</br> | |
- | 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.</br> |
- | 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.</br> |
- | 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).</br> |
- | 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</br> |
- | 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.</br> |
- | 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.</br></p> |
- | 9. Add 50~100μl Elution Buffer and collect the plasmid. | + | <div style="width:580px;height:655px;border-radius:1em 1em 1em 1em;background:#ffffff;border:1px solid rgb(68,68,68);padding:5px;"> |
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- | + | <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;"> |
+ | <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> | ||
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+ | <img src="https://static.igem.org/mediawiki/2013/7/7d/Prep31_%E5%89%AF%E6%9C%AC.png" width="231" height="208" /> </div> | ||
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<div class="port-sidebar-border"><h>notebook</h></div> | <div class="port-sidebar-border"><h>notebook</h></div> | ||
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Latest revision as of 16:50, 27 September 2013