Team:Newcastle/15 July 2010

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#*double digests with Pst1 and Xba1
#*double digests with Pst1 and Xba1
#Gel electrophoresis - the [[Team:Newcastle/Gel_electrophoresis|gel electrophoresis]] protocol was followed.  
#Gel electrophoresis - the [[Team:Newcastle/Gel_electrophoresis|gel electrophoresis]] protocol was followed.  
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#Set up liquid broth culture in 5 ml of LB - 1 colony from colonies 1-7. The protocol for [[Team:Newcastle/Growing_an_overnight_cultures| growing an overnight culture]] was followed.
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Set up liquid broth culture in 5 ml of LB - 1 colony from colonies 1-7
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{{Team:Newcastle/footer}}
{{Team:Newcastle/footer}}

Revision as of 06:42, 9 August 2010

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LacI BioBrick Construction

Aims

  • To use PCR to extract lacI (promoter, ribosome-binding site (RBS) & coding sequence (CDS)) from plasmid pMutin4 and ligate into vector pSB1AT3 in front of red fluorescent protein (RFP).
  • The aim of today's experiment is to screen for the lacI insert. The experiments that were carried out yesterday are being repeated today as there were extra and unexpected bands on the image of the gel.

Protocol

  1. Miniprep - the miniprep protocol was followed.
  2. Restriction digests - the restriction digests protocol was followed to allow the length of the DNA to be checked using single and double digest.
    • Single digest with Pst1
    • double digests with Pst1 and Xba1
  3. Gel electrophoresis - the gel electrophoresis protocol was followed.
  4. Set up liquid broth culture in 5 ml of LB - 1 colony from colonies 1-7. The protocol for growing an overnight culture was followed.
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