Team:USTC CHINA/Notebook/Protocols/Plasmid mini-prep
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- | <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> |
- | 9. Add 50~100μl Elution Buffer and collect the plasmid. | + | |
Revision as of 17:14, 25 September 2013