Difference between revisions of "Team:ITB Indonesia/Notebook"

Line 42: Line 42:
 
                         <li>Mix the following component in a PCR tube, for step I PCR</li>
 
                         <li>Mix the following component in a PCR tube, for step I PCR</li>
 
                         <img src="https://static.igem.org/mediawiki/2017/2/25/RF_1.JPG" height="50%" width="50%">
 
                         <img src="https://static.igem.org/mediawiki/2017/2/25/RF_1.JPG" height="50%" width="50%">
 +
                        <li>Quick-spin  the PCR tube, then place on the thermal cycler</li>
 +
                        <li>Set the PCR cycle profile as follow and then run as follows</li>
 +
                        <img src="https://static.igem.org/mediawiki/2017/3/31/RF_2.JPG" height="50%" width="50%">
 +
                        <li>Confirm the amplicon by running the product on 1% agarose gel, 70V for 35 minutes</li>
 +
                        <li>If positive, continue to purified PCR product using GenepHlow Gel/PCR Purification Kit (Promega)</li>
 +
                        <li>Mix the following component in a PCR tube for step II PCR</li>
 +
                        <img src="https://static.igem.org/mediawiki/2017/e/ef/RF_6.JPG" height="50%" width="50%">
 +
                        <li>Quick spin the PCR tube, the place on the thermal cycler</li>
 +
                        <li>Set the PCR cycle profile as follow and the run</li>
 +
 +
 
 
                          
 
                          
  

Revision as of 02:00, 2 November 2017

Team Attributions
Collaborations Overview Design Notebook Contribution Results Improve
Basic Parts Composite Part Part Collection
Silver HP Integrated and Gold Public Engagement


Notebook


Notebook

Protocols used in this study

  1. Basic Protocols
    • Plasmid Isolation Using Alkaline Lysis Method
      1. Inoculate transformed cell into LB medium supplemented with appropriate antibiotics
      2. Incubate culture at 37˚C, 200 rpm for overnight
      3. Discard supernatan, and repeat the step until all culture is used
      4. Add 100 µl Alkaline Lysis Solution I (0.05 M glucose; 0.025 M Tris-Cl pH 8.0; 0.01 EDTA pH 8.0) and resuspend cell pellet completely
      5. Add 200 µl Alkaline Lysis Solution II (0.2 N NaOH; 1% SDS), and invert tube several times. The solution should turn into transparent white, indicating the cell is lysed
      6. Add 150 µl Alkaline Lysis Solution III (3M Pottasium Acetate pH 7.2; 11.5% Glacial Acetate), and invert tube several times. The chromosomal DNA should make white floating thread
      7. Incubate on ice for 3-5 minutes
      8. Centrifuge at full speed for 5 minutes. At this point, plasmid DNA is dissolved in the supernatan while chromosomal DNA turn into white precipitate on the bottom of the tube
      9. Transfer supernatan to a new 1.5 microtube, add 2X volumes of isopropanol/absolute ethanol to precipitate plasmid DNA
      10. Centrifuge at full speed for 5 minutes, and discard supernatan
      11. Add 500 µl 70% ethanol to precipitated DNA
      12. Centrifuge at full speed for 5 minutes, and discard supernatan
      13. Let the precipitated DNA dreid by putting the microtube upside-down on a piece of tissue paper
      14. Resuspend plasmid by adding 50 µl TE buffer/Nuclease Free Water
    • Polymerase Chain Reaction for Restriction-Free Cloning
      1. Mix the following component in a PCR tube, for step I PCR
      2. Quick-spin the PCR tube, then place on the thermal cycler
      3. Set the PCR cycle profile as follow and then run as follows
      4. Confirm the amplicon by running the product on 1% agarose gel, 70V for 35 minutes
      5. If positive, continue to purified PCR product using GenepHlow Gel/PCR Purification Kit (Promega)
      6. Mix the following component in a PCR tube for step II PCR
      7. Quick spin the PCR tube, the place on the thermal cycler
      8. Set the PCR cycle profile as follow and the run
      9. Milk
  2. Specialized Protocols