Difference between revisions of "Team:UiOslo Norway/Lab"

Revision as of 19:46, 25 October 2017

Protocols

1. Gibson

   Gibson assembly is an exonuclease-based method to assembly multiple DNA fragments in correct order (1). The method
   was invented in 2009 by Daniel G. Gibson, of the J. Craig Venter Institute. The assembly reaction is carried out in
   one single reaction-tube, all at once, at 50° Celsius for 15-60 minutes. The process involves three different 
   enzymatic actions. A 5’ exonuclease creates overhangs, enabling matched fragments to anneal. Then a DNA polymerase
   fills gap between the annealed strands and the 5´ end. Finally, a DNA ligase seals the gaps between the filled in 
   gap and the annealed strands. 
   
   - Modifications 

       Vinsert = x 

       Vvector = y  

       Vgibson = x+y 

       Vwater = 0µl    
 




   Incubation for 1h, not 15 min

   Before transformation: One transformation with x ul concentrated Gibsen solution and one transformation with
   Gibson solution diluted 1:3 and transformation with 3*x ul diluted Gibsen solution.




2. Transformation
• E.coli TOP10: <p>One Shot® TOP10 E. coli are provided at a transformation efficiency of 1 x 109 cfu/µg supercoiled DNA and are ideal for high-efficiency cloning and plasmid propagation. They allow stable replication of high-copy number plasmids.</p> Modifications <p>5. Incubate for exactly 30-45 seconds in the 42°C water bath. Do not mix or shake.
  7. Add 200-250 µl of rom temperatured S.O.C medium to each vial. S.O.C is a rich medium; sterile technique must be practiced to avoid contamination

• E.coli DH5Alpha: Modifications 15 and 16: Not done

</ul>




• PCR

The goal of PCR is to amplify a section of DNA of interest for DNA analysis (e.g. gene insertion, sequencing, etc). The amplification rate is exponential.

• Taq polimerase (25µl reaction):
• Phusion polymerase (20µl reaction?):







• Gel

For making a small 1% gel:

Weigh out 0.5 g of agarose and mix it with 50 ml of 1x TAE buffer in a 100 ml Erlenmeyer flask.
Dissolve the agarose by bringing the mixture to the boiling point in a microwave oven, followed by mixing (by swirling the flask). Repeat the heating and mixing until all the agarose has dissolved.
Cool the agarose solution to ~50 o C by leaving it on the bench for ~20 min (or you may accelerate the cooling by applying cold water from the tap to the outside of the flask).
Using gloves, add 5 l GelRed (10 000x). Swirl the flask gently to mix, try to avoid bubbles.
Pour the gel carefully into the mold. Bubbles may be removed/punctured by using a pipette tip.




• Miniprep

 Modifications: 

During the first attempt ethanol was not added to the PE buffer, which resulted in an unsuccessful miniprepl
In the second attempt 72/4% ethanol was added, as opposed to the recommended 96-100%, resulting in a successful miniprep