Team:NYMU-Taipei/lab-protocols

From 2011.igem.org

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#Lysis: Add 200 µl of PD2 Buffer and mix gently by inverting the tube 10 times. Do not vortex to avoid shearing the genomic DNA. Let stand at room temperature for at least 2 minutes to ensure the lysate is homologous.  
#Lysis: Add 200 µl of PD2 Buffer and mix gently by inverting the tube 10 times. Do not vortex to avoid shearing the genomic DNA. Let stand at room temperature for at least 2 minutes to ensure the lysate is homologous.  
#Neutralizatio: Add 300 µl of PD3 Buffer and mix immediately by inverting the tube 10 times. Do not vortex. Centrifuge at 14-16,000 x g for 3 minutes.  
#Neutralizatio: Add 300 µl of PD3 Buffer and mix immediately by inverting the tube 10 times. Do not vortex. Centrifuge at 14-16,000 x g for 3 minutes.  
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#DNA Binding: Place a PD Column in a 2 ml Collection Tube. Add the supernatant from Step 4 to the PD Column and centrifuge at 14-16,000 x g for 30 seconds.  
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#DNA Binding: Place a PD Column in a 2 ml Collection Tube. Add the supernatant from Step 4 to the PD Column and centrifuge at 14-16,000 x g for 30 seconds. Discard the flow-through and place the PD Column back in the 2 ml Collection Tube.  
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Discard the flow-through and place the PD Column back in the 2 ml Collection  
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#Wash: Add 400 µl of W1 Buffer into the PD Column. Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow-through and place the PD Column back in the 2 ml Collection Tube. Add 600 µl of Wash Buffer (ethanol added) into the PD Column. Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow through and place the PD Column back in the 2 ml Collection Tube. Centrifuge at 14-16,000 x g again for 3 minutes to dry the column matrix.
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Tube.  
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#Wash: Add 400 µl of W1 Buffer into the PD Column. Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow-through and place the PD Column back in the 2 ml Collection Tube. Add 600 µl of Wash Buffer (ethanol added) into the PD Column.
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Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow through and place the PD Column back in the 2 ml Collection Tube. Centrifuge at 14-16,000 x g again for 3 minutes to dry the column matrix.
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#DNA Elution: Transfer the dried PD Column to a new microcentrifuge tube. Add 50 µl of Elution Buffer or TE into the center of the column matrix. Let stand for at least 2 minutes to allow the Elution Buffer or TE to be completely absorbed. Centrifuge at 14-16,000 x g for 2 minutes to elute the DNA.
#DNA Elution: Transfer the dried PD Column to a new microcentrifuge tube. Add 50 µl of Elution Buffer or TE into the center of the column matrix. Let stand for at least 2 minutes to allow the Elution Buffer or TE to be completely absorbed. Centrifuge at 14-16,000 x g for 2 minutes to elute the DNA.
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Revision as of 21:10, 5 October 2011

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Contents

General

Transformation

ECOS(sup)TM(/sup) One-minute competent cells

  1. Prepare 42 degree Celsius water bath, plating beads and selective plates. Thaw frozen competent cells in -80 degree Celsius with room-temp. Water bath to obtain approximately 1/3 thawed state.
  2. Add DNA (DNA in 4 degree Celsius or ice-bathed plasmids or ligation mixture), whose total volume is less than 5% of volume of competent cells and vortex for 1 second. Wait 5 minutes.
  3. Incubate in 42 degree Celsius water bath for 45 seconds.
  4. Transfer onto chilled and dry selection plate media, then spread the competent cells.
  5. Immediately incubate plate at 37 degree Celsius for 12-16 hours.

High-Speed Plasmid Mini Kit Protocol

Geneaid High-Speed Plasmid Mini Kit

Add provided RNase A to the PD1 Buffer and store at 4ºC; if precipitates have formed in the PD2 Buffer, warm the buffer in a 37ºC water bath, followed by gentle shaking to dissolve. Add absolute ethanol (see the bottle label for volume) to the Wash Buffer prior to initial use.

  1. Harvesting: Transfer cultured bacterial cells to a 1.5 ml microcentrifuge tube. Centrifuge at 14-16,000 x g for 1 minute and discard the supernatant. Repeat this step if necessary.
  2. Re-suspension: Add 200 µl of PD1 Buffer (RNase A added) to the tube and re-suspend the cell pellet by vortex or pipetting.
  3. Lysis: Add 200 µl of PD2 Buffer and mix gently by inverting the tube 10 times. Do not vortex to avoid shearing the genomic DNA. Let stand at room temperature for at least 2 minutes to ensure the lysate is homologous.
  4. Neutralizatio: Add 300 µl of PD3 Buffer and mix immediately by inverting the tube 10 times. Do not vortex. Centrifuge at 14-16,000 x g for 3 minutes.
  5. DNA Binding: Place a PD Column in a 2 ml Collection Tube. Add the supernatant from Step 4 to the PD Column and centrifuge at 14-16,000 x g for 30 seconds. Discard the flow-through and place the PD Column back in the 2 ml Collection Tube.
  6. Wash: Add 400 µl of W1 Buffer into the PD Column. Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow-through and place the PD Column back in the 2 ml Collection Tube. Add 600 µl of Wash Buffer (ethanol added) into the PD Column. Centrifuge at 14-16,000 x g for 30 seconds. Discard the flow through and place the PD Column back in the 2 ml Collection Tube. Centrifuge at 14-16,000 x g again for 3 minutes to dry the column matrix.
  7. DNA Elution: Transfer the dried PD Column to a new microcentrifuge tube. Add 50 µl of Elution Buffer or TE into the center of the column matrix. Let stand for at least 2 minutes to allow the Elution Buffer or TE to be completely absorbed. Centrifuge at 14-16,000 x g for 2 minutes to elute the DNA.

RE Digestion

- 15μl DNA -0.5μl E1 -0.5μl E2 -2μl 10X buffer -2μl H2O -20 μl total

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