Team:Wash U/Calendar-Home/14 July 2009

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-Performed Triligation and Silver Lab Ligations to fuse OmpC+GFP <br>
-Performed Triligation and Silver Lab Ligations to fuse OmpC+GFP <br>
-Started cultures of dbcOmega in LB+Strep in lieu of ATCC <br>
-Started cultures of dbcOmega in LB+Strep in lieu of ATCC <br>
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Gel #1: Silver digestion protocol
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1) Ladder
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2) OmpC + pSB1A2 plasmid (2187 bp)
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3) OmpC + pSB1A2 plasmid
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4) GFP (876 bp)
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5) GFP
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6) Ladder
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Gel #2: BioBrick (Triligation) digestion protocol
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1) Ladder
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2) OmpC (108 bp)
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3) OmpC
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4) Destination plasmid, pSB1K3 (2206 bp)
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5) Dest. plasmid, pSB1K3
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6) GFP (876 bp)
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7) GFP
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8) Ladder
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[[Team:Wash_U/Calendar-Home/9 July 2009|Previous entry]]</div>
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[[Team:Wash_U/Calendar-Home/13 July 2009|Previous entry]]</div>
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Latest revision as of 16:43, 15 July 2009

Tuesday, July 14, 2009

-Colony PCR of cells transformed with previous ligations
-PCR to add KpnI and BamHI sites to GFP
-Spectrophotometry of dbcOmega strains in ATCC media
-PCR to add BioBrick prefix and suffix to Cph8 and pRKCBC3
-Transformed S17 competent cells to check efficiency. OD = 0.115
-Performed Triligation and Silver Lab Ligations to fuse OmpC+GFP
-Started cultures of dbcOmega in LB+Strep in lieu of ATCC

Gel #1: Silver digestion protocol

1) Ladder

2) OmpC + pSB1A2 plasmid (2187 bp)

3) OmpC + pSB1A2 plasmid

4) GFP (876 bp)

5) GFP

6) Ladder

Gel #2: BioBrick (Triligation) digestion protocol

1) Ladder

2) OmpC (108 bp)

3) OmpC

4) Destination plasmid, pSB1K3 (2206 bp)

5) Dest. plasmid, pSB1K3

6) GFP (876 bp)

7) GFP

8) Ladder


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