Team:Paris/August 20
From 2008.igem.org
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*Overnight incubation (37°C) | *Overnight incubation (37°C) | ||
- | ='''Miniprep and stock glycerol'''= | + | ='''Miniprep and stock glycerol of stable strains with biobricks 2008'''= |
*[[Team:Paris/Notebook/Protocols#Glycerol stocks| Protocol stocks]] | *[[Team:Paris/Notebook/Protocols#Glycerol stocks| Protocol stocks]] | ||
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|} | |} | ||
- | => Following a mistake, the right E0430(D166) and E0432(D167) digestion, have not been purified. | + | => Following a mistake, the right E0430(D166) and E0432(D167) digestion, have not been purified. <br>So we need to repeat the same digestion experiment tomorrow morning. |
- | So we need to repeat the same digestion experiment tomorrow morning. | + | |
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+ | ='''Construction of: promotor-rbs-LasR-dbl ter'''= | ||
+ | ==Results of the transformation we did [[Team:Paris/August 18 |the day before yesterday]]== | ||
+ | ===Number of colonies=== | ||
{|border="1" style="text-align: center" | {|border="1" style="text-align: center" | ||
|'''Ligation name''' | |'''Ligation name''' | ||
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|} | |} | ||
- | + | ==PCR Screening== | |
- | == | + | [[Team:Paris/Notebook/Protocols#PCR Screening| Protocol]] |
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[[Image:J23100-J23101+D165.jpg |thumb| Ligations results J23100+D165 and J23101+D165]] | [[Image:J23100-J23101+D165.jpg |thumb| Ligations results J23100+D165 and J23101+D165]] | ||
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{|border="1" style="text-align: center" | {|border="1" style="text-align: center" | ||
|'''Well''' | |'''Well''' | ||
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- | | | + | |17 |
|- | |- | ||
- | | | + | |'''Sample''' |
- | |L154.8 | + | |colspan="8" |L153 |
+ | |1kb ladder | ||
+ | |colspan="8" |L154 | ||
+ | |- | ||
+ | |'''Clone''' | ||
+ | |.1 | ||
+ | |.2 | ||
+ | |.3 | ||
+ | |.4 | ||
+ | |.5 | ||
+ | |.6 | ||
+ | |.7 | ||
+ | |.8 | ||
+ | | | ||
+ | |.1 | ||
+ | |.2 | ||
+ | |.3 | ||
+ | |.4 | ||
+ | |.5 | ||
+ | |.6 | ||
+ | |.7 | ||
+ | |.8 | ||
+ | |- | ||
+ | |'''Expected size''' | ||
+ | |colspan="8" |1194 | ||
+ | | | ||
+ | |colspan="8" |1194 | ||
+ | |- | ||
+ | |'''Measured size''' | ||
+ | |style="background: #cbff7B" colspan="8" |1200 | ||
+ | | | ||
+ | |style="background: #cbff7B" colspan="8" | 1200 | ||
|} | |} | ||
- | == | + | ==Minipreps== |
{|border="1" style="text-align: center" | {|border="1" style="text-align: center" | ||
|'''Miniprep Name''' | |'''Miniprep Name''' | ||
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- | =Promoter characterization plasmids= | + | ='''Promoter characterization plasmids'''= |
- | + | ||
==Ligation== | ==Ligation== | ||
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Our ligations from yesterday didn't work. The positive control for transformation worked. | Our ligations from yesterday didn't work. The positive control for transformation worked. | ||
==Digestion== | ==Digestion== | ||
- | + | We had a problem with a gel extraction so we have to make again the digestions from yesterday, Other digestions made: | |
- | We had a problem with a gel extraction so we have to make again the digestions from yesterday | + | |
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- | Other digestions made: | + | |
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- | + | ||
[[Team:Paris/Notebook/Protocols#Digestion|Protocol Digestion]] | [[Team:Paris/Notebook/Protocols#Digestion|Protocol Digestion]] | ||
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D183 | D183 | ||
[[Image:20-08-08.png|200px]] | [[Image:20-08-08.png|200px]] | ||
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D184 | D184 | ||
D185 | D185 | ||
[[Image:20-08-08bis.png|100px]] | [[Image:20-08-08bis.png|100px]] | ||
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='''Sequencing'''= | ='''Sequencing'''= | ||
*We received results of our sequencing from COCHIN | *We received results of our sequencing from COCHIN | ||
- | *We succeed for FlgA promoter | + | *We succeed for FlgA promoter |
- | * FlgB and flhB don't match with our expected sequences. We decided to cut our Miniprep product with other enzymes to check our sequence. | + | *FlgB and flhB don't match with our expected sequences.<br>We decided to cut our Miniprep product with other enzymes to check our sequence. |
- | + | ==Digestion== | |
- | == | + | |
[[Team:Paris/Notebook/Protocols#Digestion |Protocol]] | [[Team:Paris/Notebook/Protocols#Digestion |Protocol]] | ||
*D176 : pFlgB digested with ApoI | *D176 : pFlgB digested with ApoI | ||
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*D178 : pFlhB digested with BstAPI | *D178 : pFlhB digested with BstAPI | ||
- | = | + | ==Screening== |
- | [[Image:Gel1 FlgB.jpg | | + | Gel 1 [[Image:Gel1 FlgB.jpg |150px]] Gel 2[[Image:Gel_2_FlhB.2.jpg |150px]] |
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+ | |||
{|border="1" style="text-align: center" | {|border="1" style="text-align: center" | ||
+ | | | ||
+ | |colspan="8"|'''Gel 1''' | ||
+ | |colspan="9"|'''Gel 2''' | ||
+ | |- | ||
|'''Well''' | |'''Well''' | ||
|1 | |1 | ||
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|- | |- | ||
|'''Sample''' | |'''Sample''' | ||
- | | | + | |1kb<br>ladder |
+ | |D176.1 | ||
+ | |D176.2 | ||
+ | |D176.3 | ||
+ | |D176.4 | ||
+ | |D177.1 | ||
+ | |D177.2 | ||
+ | |100pb<br>ladder | ||
+ | |no sample | ||
|D177.3 | |D177.3 | ||
|D177.4 | |D177.4 | ||
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|D178.3 | |D178.3 | ||
|D178.4 | |D178.4 | ||
- | |1kb ladder | + | |1kb<br>ladder |
|- | |- | ||
|'''Expected size''' | |'''Expected size''' | ||
+ | | | ||
+ | |colspan="4" |2970<br>194<br>48 | ||
+ | |colspan="2" |3212 | ||
| | | | ||
|colspan="2" |3212 | |colspan="2" |3212 | ||
- | |colspan=" | + | |colspan="5" |3213 |
|- | |- | ||
|'''Measured size''' | |'''Measured size''' | ||
| | | | ||
- | |colspan=" | + | |style="background: #cbff7B" colspan="4" |2900<br>200<br>/ |
+ | |style="background: #ff6d73" colspan="2" |Plamsid not digested | ||
+ | | | ||
+ | |style="background: #ff6d73" colspan="7" |Plamsid not digested | ||
| | | | ||
|} | |} | ||
- | Conclusion => the sequence of pFlgB and pFlhB are not good we will tried to isolate pFlhB again. | + | Conclusion => the sequence of pFlgB and pFlhB are not good we will tried to isolate pFlhB again. |
Latest revision as of 14:03, 6 September 2008
Screening of the cloning of E0240 and FlhDC+promotorSpreading the clones in order to obtain single colonies
The plates obtained from the speading of yesterday can't be used because there are not single colonies.
Miniprep and stock glycerol of stable strains with biobricks 2008Construction for FIFOAim : Construction of pFlgA - YFP tripart (+/- LVA) "pFlgA-RBS-YFP-dbl ter" (pFlgA-E0430/E0432) DigestionMeasurement of concentration of minipreps
Digestion
Gel Extraction
=> Following a mistake, the right E0430(D166) and E0432(D167) digestion, have not been purified.
Construction of: promotor-rbs-LasR-dbl terResults of the transformation we did the day before yesterdayNumber of colonies
PCR Screening
Minipreps
Promoter characterization plasmidsLigationOur ligations from yesterday didn't work. The positive control for transformation worked. DigestionWe had a problem with a gel extraction so we have to make again the digestions from yesterday, Other digestions made:
Sequencing
*We succeed for FlgA promoter *FlgB and flhB don't match with our expected sequences. Digestion
Screening
Conclusion => the sequence of pFlgB and pFlhB are not good we will tried to isolate pFlhB again. |