Template:SBB10 ConstructionFiles AmyK sbb22

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Construction of FokI- basic part	
 PCR ak10F/ak20R     Registry part BBa_K243001            (230 bp, gp = A)
 PCR ak20F/ak30R     Registry part BBa_K243001            (71 bp, gp = B)
 PCR ak30F/ak40R     Registry part BBa_K243001            (245 bp, gp = C)
 PCR ak40F/ak11R     Registry part BBa_K243001            (135 bp, gp = D)
 ---------------------------------------------------
 PCR ak10F/ak11R on A+B+C+D           (619bp, EcoRI/BamHI)
 Digest pBjk2741-Bca1144              (EcoRI/BamHI, 910+2170, L)
 Product is pBjk2741-Bak1234  {<FokI->}
 ---------------------------------------------------
 ak10F  Forward EcoRI for FokI- CCATAgaattcCAGagatctCAGCTGGTTaaatctgaactggaggagaa 
 ak20F  Base substitution 1  gtaaaccagACggtgccatt
 ak20R  Base substitution 1  aatggcaccGTctggtttac
 ak30F  Base substitution 2  cgttatcgtggAcacaaaagcg
 ak30R	Base substitution 2  cgcttttgtgTccacgataacgc
 ak40F  Base substitution 3  caccaatTgcaatggggcag
 ak40R  Base substitution 3  ctgccccattgcAattggtg
 ak11R  Reverse BamHI for FokI- CTGATggatccaaaattgatctcgccattg

JCA Notes

  • Assembles fine
  • Changed seq on Clotho, restriction sites were included
  • Name of part should be sbb22, changed wikilink, and corrected file
  • Due to similarity to another part, shared some oligos
Construction of FokI- basic part	
 PCR gh1000F/gh1001R on BBa_K243001   (261 bp, gp = A)
 PCR gh1001F/gh1003R on BBa_K243001   (264 bp, gp = B)
 PCR gh1003F/ak11R     Registry part BBa_K243001            (141 bp, gp = C)
 ---------------------------------------------------
 PCR gh1000F/ak11R on A+B+C           (619bp, EcoRI/BamHI)
 Digest pBjk2741-Bca1144              (EcoRI/BamHI, 910+2170, L)
 Product is pBjk2741-sbb22   {<FokI->}
 ---------------------------------------------------
 gh1000F  Forward for part <FokI-!    ccagtGAATTCatgAGATCTCAGCTGGTTaaatctgaactggaggag
 gh1001F  Making internal mutation 1+2 cgttggttccccgatcgattatggcgttatcgtggAcacaaaagc
 gh1001R  Making internal mutation 1+2 cgccataatcgatcggggaaccaacggtataaatggcaccGTctggtttac
 gh1003F  Making internal mutation 3   ccatatcaccaatTgcaatggggcagtgctgag
 gh1003R  Making internal mutation 3   ccattgcAattggtgatatgg
 ak11R  Reverse BamHI for FokI- CTGATggatccaaaattgatctcgccattg