Team:Paris Saclay/Notebook/July/8

From 2013.igem.org

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{{Team:Paris_Saclay/incl_debut_generique}}
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='''Notebook : July 8'''=
='''Notebook : July 8'''=
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==''Summary:''==
 
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FNR regulator system:
 
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*performed another digestion for AmilCP, Pfnr plus sequence LacZ with Not I, Xho I, EcoR I and PST I.
 
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*electrophoresis for those digest products
 
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*enrichment culture for clone of the briobrick BBa_K1155000
 
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*electrophoresis for extracted products of last friday
 
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=='''Lab work'''==
 
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Overnight incubation at 37°C with agitation.
 
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<br>
 
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The electrophoresis for the plasmids which we had extracted last week plus 3 other BioBrick promoter Bph R1, promoter Bph A1, Bph R2.
 
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Volume added:
 
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*Pfnr2: 10µl
 
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*R1P: 10µl
 
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*R2: 10µl
 
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*A1P: 10µl
 
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Migration at 100V for 25mins then continued till 45 minutes:
 
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<br>
 
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Results:
 
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{| align="center"
 
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| style="width:350px;border:1px solid black;" | [[File:PS08071345.jpg|right|350px]]
 
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| style="width:350px;border:1px solid black;" |
 
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*Well 1 : R2
 
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*Well 2 : R1P
 
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*Well 3 : A1P
 
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*Well 4 : Pfnr
 
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*gel 0.8%
 
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|}<br>
 
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The concentration of Pfnr2 was detected by NanoDrop :
 
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*C = 1788.8 ng/µl
 
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*260/280 = 2.08
 
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We considered that our extraction of plasmid DNA was not successful, we need to perform another extraction DNA.
 
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<u>Electrophoresis band size estimation</u><br>
 
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<p>We used Clonemanager for band size estimation:</p>
 
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<br>
 
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{| border="1" align="center"
 
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|-
 
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|Molecule
 
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|enzymes(Buffer)
 
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|Size
 
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|BBa_K1155000
 
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|XHOI(Red)
 
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|1289+892bp
 
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|BBa_K1155000
 
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|ECoR I(Orange)
 
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|2151bp
 
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|}<br>
 
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{{Team:Paris_Saclay/incl_debut_generique}}
 
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='''Notebook : August 23'''=
 
=='''Lab work'''==
=='''Lab work'''==

Revision as of 15:04, 26 September 2013

Contents

Notebook : July 8

Lab work

A - Aerobic/Anaerobic regulation system

Objective : Bba_K1155003, Bba_K1155007

1 - Digestion of Bba_K592009, Bba_K1155007 by NotI, XhoI, EcoRI, EcoRI/PstI

Abou, Anaïs, Sheng, Zhou

Used quantities :

  • NotI :
    • Bba_K592009 : 2µL
    • Buffer orange : 2µL
    • NotI : 0.5µL
    • H2O : 15.5µL
  • XhoI :
    • Bba_K592009 : 2µL
    • Buffer red : 2µL
    • XhoI : 0.5µL
    • H2O : 15.5µL
  • EcoRI :
    • Bba_K592009 : 2µL
    • Buffer orange : 2µL
    • EcoRI : 0.5µL
    • H2O : 15.5µL
  • EcoRI/PstI :
    • Bba_I732017 : 2µL
    • Buffer orange : 2µL
    • EcoRI : 0.5µL
    • PstI : 0.5µL
    • H2O : 15µL

We let our digestion 1h30 at 37°C.

2 - Electrophoresis of the digestion of Bba_K592009, Bba_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI

Abdou, Anaïs, Sheng, Zhou

[[]]
  • Well 1 : 6µL DNA Ladder
  • Well 2 : 5µL Bba_K592009 clone 1 digested by EcoRI+1µl of 6X loading dye
  • Well 3 : 5µL Bba_K592009 clone 2 digested by EcoRI+1µl of 6X loading dye
  • Well 4 : 5µL Bba_K592009 clone 1 digested by NotI+1µl of 6X loading dye
  • Well 5 : 5µL Bba_K592009 clone 2 digested by NotI+1µl of 6X loading dye
  • Well 6 : 5µL Bba_K592009 clone 1 digested by XhoI+1µl of 6X loading dye
  • Well 7 : 5µL Bba_K592009 clone 2 digested by XhoI+1µl of 6X loading dye
  • Well 8 : 5µL Bba_I732017 clone 1 digested by EcoRI/PstI+1µl of 6X loading dye
  • Well 9 : 5µL Bba_I732017 clone 2 digested by EcoRI/PstI+1µl of 6X loading dye
  • Well 10 : -
  • Well 11 : -
  • Well 12 : 6µL DNA Ladder
  • Gel : 1%

Expected sizes :

  • Bba_K592009 digested by NotI : 2046bp + 693bp
  • Bba_K592009 digested by XhoI : 1842bp + 892bp
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