Template:Team:KULeuven/24 August 2009/BlueLightReceptor

From 2009.igem.org

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# platen met ligatie A zijn onder het blauw licht gezet. De LEDs werden op maximum gezet.  
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# Plates with LigA were put under blue light. The LEDs were put on their max capacity.  
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# restriction digest with  
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# Restriction digest with  
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#*tubes (1,3,5,7,9) of ligA (BLP + E0240) cut with EcoRI en PstI
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#*tubes (1,3,5,7,9) of LigA (BLP + {{kulpart|BBa_E0240}}) cut with EcoRI en PstI
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#*promotor J23101 cut with EcoRI en SpeI (4x)
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#*promotor {{kulpart|BBa_J23101}} cut with EcoRI en SpeI (4x)
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#gel electroforese with the RD of ligA and J23101 followed by a gel extraction:
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#Gel electrophoresis with the RD of LigA and {{kulpart|BBa_J23101}} followed by a gel extraction:
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#* note: tube 5 of ligA was loaded poorly on the gel and could not be used.
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#* Note: tube 5 of LigA was loaded poorly on the gel and could not be used.
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#* note: the samples of promotor J23101 were barly visible. only 2 of the 4 samples were recoverd by extraction.  
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#* Note: the samples of promotor {{kulpart|BBa_J23101}} were barely visible. Only 2 of the 4 samples were recovered by extraction.  
{| border ="1" align="center"
{| border ="1" align="center"
!| Part || concentration (ng/μl) || 260/280 λ ||  
!| Part || concentration (ng/μl) || 260/280 λ ||  
|- align="center"
|- align="center"
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| ligA 1 ||7,9 || 2,16 ||
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| LigA 1 ||7,9 || 2,16 ||
|- align="center"
|- align="center"
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| ligA 3 ||10,8 || 1,88 ||
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| LigA 3 ||10,8 || 1,88 ||
|- align="center"
|- align="center"
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| ligA 7 ||4,8 || 2,49 ||
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| LigA 7 ||4,8 || 2,49 ||
|- align="center"
|- align="center"
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| ligA 9 ||8,0 || 3,02 ||  
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| LigA 9 ||8,0 || 3,02 ||  
|- align="center"
|- align="center"
| {{kulpart|BBa_J23101}} (A) ||20,8|| 1,70 ||
| {{kulpart|BBa_J23101}} (A) ||20,8|| 1,70 ||
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| {{kulpart|BBa_J23101}} (B) ||12,8|| 2,57 ||
| {{kulpart|BBa_J23101}} (B) ||12,8|| 2,57 ||
|}
|}
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3.enting of liquid cultures with kanamycin and pSB3K3
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4. Enting of liquid cultures with kanamycin and {{kulpart|pSB3K3}}

Latest revision as of 12:25, 14 September 2009

  1. Plates with LigA were put under blue light. The LEDs were put on their max capacity.
  2. Restriction digest with
    • tubes (1,3,5,7,9) of LigA (BLP + ) cut with EcoRI en PstI
    • promotor cut with EcoRI en SpeI (4x)
  3. Gel electrophoresis with the RD of LigA and followed by a gel extraction:
    • Note: tube 5 of LigA was loaded poorly on the gel and could not be used.
    • Note: the samples of promotor were barely visible. Only 2 of the 4 samples were recovered by extraction.
Part concentration (ng/μl) 260/280 λ
LigA 1 7,9 2,16
LigA 3 10,8 1,88
LigA 7 4,8 2,49
LigA 9 8,0 3,02
(A) 20,8 1,70
(B) 12,8 2,57

4. Enting of liquid cultures with kanamycin and