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Team:Lyon-INSA-ENS/Realisation/Week13
From 2011.igem.org
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| - | + | <p style=" line-height : 1.5em"> | |
| + | <FONT COLOR="red"> <b>Transformations and controls for future tests</b> </FONT> <br/><br/> | ||
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| + | </p> | ||
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| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="blue"><b>Plasmid and strain Collection</b></FONT> <br/><br/> | ||
| + | Start of a 5mL liquid culture of S17 in LB+Cm medium<br/> | ||
| + | Minipreps of this culture to extract pIG25 in larger quantity. Digestion (E+P) and electrophoresis for control : the insert is too small, not correct. | ||
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| + | </p> | ||
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| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="purple"><b> Adherence Test Preparation </b></FONT> <br/><br/> | ||
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| + | </p> | ||
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| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="orange"> <b> Others </b></FONT> <br/><br/> | ||
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</p> | </p> | ||
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| - | + | <p style=" line-height : 1.5em"> | |
| - | + | <FONT COLOR="red"> <b>Transformations and controls </b> </FONT> <br/><br/> | |
| + | The Ptrc strong promoter has been received from Genecust in pBluescriptIISK+: transformation in MC4100 and plating on LB+Amp medium.<br/><br/> | ||
| + | |||
| + | Digestion by E+P of this plasmid and ligation into pSB1C3 overnight<br/><br/> | ||
| + | |||
| + | Plating of PHL916 on LB ( sureE strain that should not recombine DNA ) in case the transformation of pIG25 into MC4100 fails. <br/><br/> | ||
| + | |||
| + | </p> | ||
| + | |||
| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="blue"><b>Plasmid and strain Collection</b></FONT> <br/><br/> | ||
| + | |||
| + | |||
| + | </p> | ||
| + | |||
| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="purple"><b> rcn-OmpR234 adherence test </b></FONT> <br/><br/> | ||
| + | Start of a rcn-OmpR234 24 well plate with :<br/> | ||
| + | S27 ( rcn in pSB1C3 ) without cobalt and with cobalt (25µM) <br/> | ||
| + | S33 ( rcn-OmpR234 in pSB1C3 ) with increasing concentration of cobalt (0, 10, 25 and 100 µM) | ||
| + | |||
| + | |||
| + | </p> | ||
| + | |||
| + | <p style=" line-height : 1.5em"> | ||
| + | <FONT COLOR="orange"> <b> Others </b></FONT> <br/><br/> | ||
| + | Plating of PHL644, PHL1256, PHL628 to be sent to other research teams, on request.<br/><br/> | ||
| + | |||
| + | </p> | ||
<br/> <br/> | <br/> <br/> | ||
Revision as of 08:21, 15 September 2011
Week 13
From Monday the 12th of September to Friday the 16th of September 2011
Monday
Transformations and controls for future tests
Plasmid and strain Collection
Plating of S17 from the collection to extract a bigger quantity of pIG25 ( pSB1C3 containing rcn-csgBAEFG )
Storage of the correct clone of:
PHL1414 + pIG3 (S30)
PHL1414+pIG16 (S31)
MC4100 + pIG34 (S32)
Storage of rcn-OmpR in psB1K3 (pIG34) from the previous miniprep.
Adherence Test Preparation
Others
Pouring of 9 LB+Amp plates
Dilution of 5µL pIG25 (371.4 ng/µL) into 25µL water to obtain 3 additional tubes at concentration of about 50ng/µL for sequencing.
Sequencing (pIG25 and pIG27) sent.
Tuesday
Transformations and controls for future tests
Plasmid and strain Collection
Start of a 5mL liquid culture of S17 in LB+Cm medium
Minipreps of this culture to extract pIG25 in larger quantity. Digestion (E+P) and electrophoresis for control : the insert is too small, not correct.
Adherence Test Preparation
Others
Wednesday
Transformations and controls
The Ptrc strong promoter has been received from Genecust in pBluescriptIISK+: transformation in MC4100 and plating on LB+Amp medium.
Digestion by E+P of this plasmid and ligation into pSB1C3 overnight
Plating of PHL916 on LB ( sureE strain that should not recombine DNA ) in case the transformation of pIG25 into MC4100 fails.
Plasmid and strain Collection
rcn-OmpR234 adherence test
Start of a rcn-OmpR234 24 well plate with :
S27 ( rcn in pSB1C3 ) without cobalt and with cobalt (25µM)
S33 ( rcn-OmpR234 in pSB1C3 ) with increasing concentration of cobalt (0, 10, 25 and 100 µM)
Others
Plating of PHL644, PHL1256, PHL628 to be sent to other research teams, on request.
Thursday
Friday
