Team:Warsaw/Calendar-Main/17 August 2009

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Assembly of endosomal detection operon

Marcin


Task 1:

Methods:

  • Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described here

Task 2:

  • Digest previously isolated plasmids to verify the correctness of the ligation

Methods:

  • Reaction mixture composition:
  •  
    1 μl purified plasmid DNA product
    0.5 μl XbaI (Fermentas)
    0.5 μl PstI (Fermentas)
    2 μl Buffer Tango (Fermentas)
    16.5 μl MQ water

Results:

Comment:

All isolated plasmids had the expected construct.


Task 3:


Task 4:

Methods:

  • Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described here

Task 5:

  • Digest previously isolated plasmids to verify the correctness of the ligation

Methods:

  • Reaction mixture composition:
  •  
    1 μl purified plasmid DNA product
    0.5 μl XbaI (Fermentas)
    0.5 μl PstI (Fermentas)
    2 μl Buffer Tango (Fermentas)
    16.5 μl MQ water

Results:

Comment:

None of isolated plasmids had the expected constructs. Ligations must be prepared once again.


Task 6:

Methods:

  • Reaction mixture composition:
  •  
    20 μl purified plasmid DNA product
    1 μl XbaI (Fermentas) or 0.5 SpeI (Fermentas)
    1 μl PstI (Fermentas)
    5 μl Buffer Tango (Fermentas)
    24 μl MQ water

Results:

Making of the plac-RBS-llo part

Jarek


Tasks:

  • Transformating the competent ''E.coli'' strain TopF' with ligation (acquired from Marek) containing RBS-llo gene cloned into vector with plac promoter
  • Plating the transformated culure on LB+Amp plates

Cloning switch 1 regulatory parts [ K177012-PcI.RBS.LacI, K177033-PcI.RBS.LacI.PcI.RBS.RFP.terminator, K177011-PLacI.RBS.cI.terminator, K177038-PLacI.RBS.cI.terminator.PLacI.RBS.GFP.terminator ] into two compatible low copy number plasmids of different antibiotic resistance

Ania


Tasks:



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