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

From 2013.igem.org

(Difference between revisions)
Line 57: Line 57:
<div class="leftbar" align="left">
<div class="leftbar" align="left">
<div class="bassic-bar">
<div class="bassic-bar">
-
<h1>Gel Extraction</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

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.