Team:Paris Saclay/Notebook/August/5

From 2013.igem.org

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We obtain fragments at the right size. We will make an elector-elution to extract RBS-LacZ.
We obtain fragments at the right size. We will make an elector-elution to extract RBS-LacZ.
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===='''3 - PCR of PSB1C3'''====
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Nadia, XiaoJing
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Used quantities :
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* PSB1C3 : 2µL
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* Buffer phusion : 10µL
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* Oligo 64 : 2.5µL
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* Oligo 65 : 2.5µL
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* dNTP : 1µL
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* Phusion : 0.25µL
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* H2O : 36.75µL
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PCR program :
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Hybridation temperature gradient :
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A - 65
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B - 64.7
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C - 64.1
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D - 63.1
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E - 62
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F - 61.2
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G - 60.5
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H - 60
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[[File:PsPCRC30508.jpg|400px]]
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===='''3 - Electrophoresis of PCR of PSB1C3'''====
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Nadia, XiaoJing
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{|
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| style="width:350px;border:1px solid black;" |[[]]
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| style="width:350px;border:1px solid black;vertical-align:top;" |
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* Well 1 : 6µL of DNA Ladder
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* Well 2 to 8 : 2µL of PSB1C3+3µL of H2O+1µL of 6X loading dye
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* Gel : 1%
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|}
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Expected sizes :
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* PSB1C3 :
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{|
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| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
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We obtain fragments at the right size. We will purify it.
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|}
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===='''4 - Gel purification of electrophoresis of PCR of PSB1C3'''====
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Nadia, XiaoJing
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Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]
===='''Objective : obtaining Bba_K1155004, Bba_K1155005, Bba_K1155006'''====
===='''Objective : obtaining Bba_K1155004, Bba_K1155005, Bba_K1155006'''====

Revision as of 16:55, 27 September 2013

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Contents

Notebook : August 5

Lab work

A - Aerobic/Anaerobic regulation system

Objective : obtaining Bba_K1155003

1 - Digestion of Bba_K1155003 by EcoRI/PstI to check the ligation between RBS-Amil CP,Term and PSB1C3

Nadia, XiaoJing

Used quantities :

  • Bba_K1155003 : 5µL
  • EcoRI FD : 1µL
  • PstI FD : 1µL
  • Buffer FD : 3µL
  • H2O : 20µL

We let the digestion at 37°C during 15 minutes.

2 - Electrophoresis of the digestion of Bba_K1155003

Damir

File:Ps.jpg|350px]]
  • Well 1 :
  • Well 2 : 6µL of DNA Ladder
  • Well 3 : 30µL of Bba_K1155003 from clone 9 digested by EcoRI/PstI+6µl of 6X loading dye
  • Well 4 : 5µL of Bba_K1155003 from clone 9+1µl of 6X loading dye
  • Well 5 : 30µL of Bba_K1155003 from clone 11 digested by EcoRI/PstI+6µl of 6X loading dye
  • Well 6 : 5µL of Bba_K1155003 from clone 11+1µl of 6X loading dye
  • Well 7 : 30µL of Bba_K1155003 from clone 12 digested by EcoRI/PstI+6µl of 6X loading dye
  • Well 8 : 5µL of Bba_K1155003 from clone 12+1µl of 6X loading dye
  • Gel : 1%

Expected sizes :

  • RBS_Amil CP-Term :
  • PSB1C3 :

CONCLUSION !!!!!!

Objective : obtaining Bba_K1155007

1 - Digestion of Bba_I732017 by EcoRI/SpeI

Abdou, Damir, Nadia,

Used quantities :

  • Bba_I732017 : 41µL
  • Buffer FD : 5µL
  • EcoRI : 2µL
  • SpeI : 2µL

We let the digestion at 1h30 at 37°C.

2 -Electrophoresis to check the digestion of Bba_I732017 by EcoRI/SpeI

Damir, Nadia

[[]]
  • Well 1 : 6µL of DNA Ladder
  • Well 2 : 40µL of Bba_I732017 digested by EcoRI/SpeI+8µL 6X loading dye
  • Gel : 1.5%

Expected sizes :

  • RBS-LacZ : 3093 bp
  • PSB1A2 : 2079 bp

We obtain fragments at the right size. We will make an elector-elution to extract RBS-LacZ.

3 - PCR of PSB1C3

Nadia, XiaoJing

Used quantities :

  • PSB1C3 : 2µL
  • Buffer phusion : 10µL
  • Oligo 64 : 2.5µL
  • Oligo 65 : 2.5µL
  • dNTP : 1µL
  • Phusion : 0.25µL
  • H2O : 36.75µL

PCR program :

Hybridation temperature gradient : A - 65 B - 64.7 C - 64.1 D - 63.1 E - 62 F - 61.2 G - 60.5 H - 60

PsPCRC30508.jpg

3 - Electrophoresis of PCR of PSB1C3

Nadia, XiaoJing

[[]]
  • Well 1 : 6µL of DNA Ladder
  • Well 2 to 8 : 2µL of PSB1C3+3µL of H2O+1µL of 6X loading dye
  • Gel : 1%

Expected sizes :

  • PSB1C3 :

We obtain fragments at the right size. We will purify it.

4 - Gel purification of electrophoresis of PCR of PSB1C3

Nadia, XiaoJing

Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]

Objective : obtaining Bba_K1155004, Bba_K1155005, Bba_K1155006

1 - Colony PCR of Bba_K1155004, Bba_K115005, Bba_K1155006 in DH5α

Damir, Nadia, XiaoJing

Transformation of 07/31/13 works. We will do a PCR Colony.

COLONIES PIQUEES DANS 10µL d'eau par Tube !!!!!!!!!!!!!

Used quantities :

  • DNA : 2µL
  • Mix  : (it was divided in 25 tubes for 25 different colonies for each promotor with 23µL of mix in each tube)
    • Oligo 44 : 3.5µL
    • Oligo 45 : 3.5µL
    • Buffer Dream Taq : 70µL
    • dNTP : 28µL
    • Dream Taq : 5µL
    • H2O : 590µL

PCR Program :

PsPCR0508.jpg


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