Team:Paris/August 11

From 2008.igem.org

(Difference between revisions)
(→PCR)
(→PCR verification/Analysis)
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* 2*3µl have been analysed by electrophoresis
* 2*3µl have been analysed by electrophoresis
* the other 44µl of PCR products have been purified by the Promega kit.
* the other 44µl of PCR products have been purified by the Promega kit.
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 +
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* '''Electrophoresis'''
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ladder : 10µl ladder 1 kb
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<br> samples : 3µl of PCR products + 2µl of Loading Dye
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<br> migration 30min at 100V, on a '''1%''' agarose gel
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* '''Results :'''
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{| border="1"
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|- style="text-align: center;"
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|'''Name'''
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|'''Promotor'''
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|align="center"|'''Band'''
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|align="center"|'''Expected size'''
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|align="center"|'''Measured size'''
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|- style="text-align: center;"
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|PCR_Control -
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|control -
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|2
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| 0 pb
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|style="background: #cbff7B"|<center> 0 pb</center>
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|}
==Culture of ligation transformants==
==Culture of ligation transformants==

Revision as of 15:36, 12 August 2008

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Contents

Transformation

Digestion

PCR

We performed PCR on to amplify the sequence in order to have enough amount of DNA to carry out the following of our experiments.


PCR amplification

Protocol

  • List of Oligos :
Number Name Sequence Length Comments
O110 FlhDC-Uri-F GTTTCTTCGAATTCGCGGCCGCTTCTAGAGTTGTATGTGCGTGTAGTGACGAGTACAG 58 Don't amplify the both OmpR binding site
O111 FlhDC-Total-F GTTTCTTCGAATTCGCGGCCGCTTCTAGAGTCATTTTTGCTTGCTAGCGTACGGAAAA 58 Amplify the both OmpR binding site
O113 FlhDC(nu)-R GTTTCTTCCTGCAGCGGCCGCTACTAGTACAGAATAACCAACTTTATTTTTATG 54 Don't amplify the natural rbs of FlhD (only promoter)
O124 Oligo-pfliL-Forward-TRO TCGAATTCGCGGCCGCTTCTAGAGCAAGGGCGTGTAACAGGCAAC 45
O125 Oligo-pfliL-Reverse-TRO TCCTGCAGCGGCCGCTACTAGTAGTCATGTGTTGCGGTCTTCCTGTG 47
O130 Gene-FlhC-F GTTTCTTCGAATTCGCGGCCGCTTCTAGATGAGTGAAAAAAGCATTGTTCAGG 53
O131 Gene-FlhC-R-TRO GTTTCTTCCTGCAGCGGCCGCTACTAGTATTATTAAACAGCCTGTACTCTCTGTTCATCC 60
O132 Gene-FlhD-F GTTTCTTCGAATTCGCGGCCGCTTCTAGATGCATACCTCCGAGTTGCTGAAAC 53 Don't amplify the natural rbs of FlhD
O133 Gene-FlhD-R-TRO GTTTCTTCCTGCAGCGGCCGCTACTAGTATTATTAGGCCCTTTTCTTGCGCAGCGCTTCT 60
O140 PlasTest_GFP_Rv CCCTGCAGTTAATTAATATAAACGCAGAAAGGCCAC 36 Amplify E0240 with a PacI and a PstI restriction site at the end
O141 PTst_GFPrbs+_F GCCTGCAGTCACACAGGAAAGTACTAGATGC 31 Amplify E0240 with the promoter and a PstI restriction site at the beginning


  • Preparation of the templates :
    Resuspension of 1 colony in 100µl of water.


  • Preparation of PCR mix :

For each sample,

1 µl dNTP
10 µl Buffer Phusion 5x
2,5 µl Oligo_F
2,5 µl Oligo_R
1µl template
1 µl Phusion
50 µl qsp H2O (33µl)


Name genes Oligo templates
PCR_130 Gel E0240 RBS+ O141_O140 MG1655
PCR_131 - O141_O140 Water
PCR_132 flhD RBS- O132_O133 MG1655
PCR_133 - O132_O133 Water
PCR_134 flhC RBS- O130_O131 MG1655
PCR_135 - O130_O131 Water
PCR_136 pflhDC O110_O131 MG1655
PCR_137 - O110_O131 Water
PCR_138 pflhDC O111_O131 MG1655
PCR_139 - O111_O131 Water
PCR_140 pfliL O124_O125 MG1655
PCR_141 - O124_O125 Water
PCR_142 pflhDC O110_O113 MG1655
PCR_143 - O110_O113 Water
PCR_144 pflhDC O111_O113 MG1655
PCR_145 - O111_O113 Water


  • Program PCR_Screening : Annealing 30" at 60°C - Time élongation 1'30" at 72°C - Number cycle : 30


PCR verification/Analysis

After the PCR :

  • 2*3µl have been analysed by electrophoresis
  • the other 44µl of PCR products have been purified by the Promega kit.


  • Electrophoresis

ladder : 10µl ladder 1 kb
samples : 3µl of PCR products + 2µl of Loading Dye
migration 30min at 100V, on a 1% agarose gel


  • Results :
Name Promotor Band Expected size Measured size
PCR_Control - control - 2 0 pb
0 pb

Culture of ligation transformants

  • 4 clones of each transformation were cultured in 7,5 mL LB + ampicilline. The colonies picked up were the rest of those already picked up from the transformation plate (for the PCR screening of August 8).
  • 37°C overnight
Ligation L128 L129 L130
Name pFlgA pFlgB pFlhB
Clone N° 1 2 3 4 1 2 6 7 1 2 7 8
Red fluorescence yes yes no no yes yes no no yes no no no
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