Team:Freiburg/Notebook

From 2012.igem.org

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{{Template:Team:Freiburg}}
{{Template:Team:Freiburg}}
__NOTOC__
__NOTOC__
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{|align="center"
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<!--- The Mission, Experiments --->
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|[[Image:smallbarfor.png|960px|no frame]]
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=Notebook =
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|}
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----
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{| style="color:#4F8DDE;background-color:#ffffff;" cellpadding="5" cellspacing="2" border="0" bordercolor="#fff" width="100%" align="left"
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<br>
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!align="center"|[[Team:Freiburg|<span style="color:#4F8DDE;">Home</span>]]
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[[File:notebooksymbolT.png|center|180px|link=]]
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!align="center"|[[Team:Freiburg/Team|<span style="color:#4F8DDE;">Team</span>]]
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<br>
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!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=Freiburg<span style="color:#4F8DDE;">Official Team Profile</span>]
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== 04/06 - 10/06 ==
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!align="center"|[[Team:Freiburg/Project|<span style="color:#4F8DDE;">Project</span>]]
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!align="center"|[[Team:Freiburg/Parts|<span style="color:#4F8DDE;">Parts Submitted to the Registry</span>]]
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!align="center"|[[Team:Freiburg/Modeling|<span style="color:#4F8DDE;">Modeling</span>]]
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!align="center"|[[Team:Freiburg/Notebook|<span style="color:#4169E1;">Notebook</span>]]
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!align="center"|[[Team:Freiburg/Safety|<span style="color:#4F8DDE;">Safety</span>]]
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!align="center"|[[Team:Freiburg/Attributions|<span style="color:#4F8DDE;">Attributions</span>]]
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|}
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{|align="center"
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|[[Image:smallbarrev.png|960px|no frame]]
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|}
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 +
:* Golden-Gate-Cloning-Reaction (GGC) to assemble a 12-repeat-TAL-TF, that recognizes the sequence TACATTGGACCTAT
 +
:* transformation: GGC-reaction
 +
:* making aliquots of ordered GGC-Primers (freiGEM-method)
 +
:* making aliquots of ordered, i.e. synthesized, direpeats
 +
:* extension-PCR of direpeats in order to produce diefferent restriction sites for correct location of direpeats
-
<!--- The Mission, Experiments --->
+
:* PCR-Purification of extension-PCR
-
=<span style="color:#2244AA"> Notebook =
+
 
 +
:* mutagenesis-PCR of Zhang-plasmid to remove restriction sites (SpeI, PstI, EcoRI, XbaI) --> making the plasmid work with iGEM-standard
 +
<br>
 +
== 11/06 - 16/06 ==
 +
 
 +
:* optimizing PCR conditions for extension of direpeats
 +
 
 +
:* redoing GGC-reaction
 +
 
 +
:* transformation of redone GGC-reaction
 +
 
 +
:* GGC á la freiGEM --> transformation
 +
 
 +
:* testing of iGEM-distribution kit
 +
<br>
 +
==  17/06 - 23/06 ==
 +
 
 +
:* cloning of direpeats into pJET 1.2 vector-system
 +
 
 +
:* colony-PCR of freiGEM-GGC product
 +
 
 +
:* place sequencing order for freiGEM-GGC
 +
 
 +
<br>
 +
==  24/06 - 01/07 ==
 +
 
 +
:* optimizing of freiGEM-GGC under various conditions
 +
 
 +
:* transformation of pJET-direpeats into bacteria
 +
 
 +
:* using the iGEM distribution kit: Bba_A12564 (CMV+Luc) --> reporter-plasmid for DNA-methyl-transferase testing
 +
 
 +
:* Miniprep of GGC-transformation (1 successful)
 +
 
 +
<br>
 +
==  02/07 - 08/07 ==
 +
 
 +
:* extension-PCR with all 96 direpeats on one well-plate
 +
 
 +
:* transformation
 +
 
 +
:* PCR-amplification of all 4 iGEM-backbones --> testing different conditions
 +
 
 +
:* making bacteria competent for transformation
 +
 
 +
<br>
 +
== 09/07 - 15/07 ==
 +
 
 +
:* digest of exDirepeats with XbaI and PstI
 +
 
 +
:* nanodrop of exDirepeats
 +
 
 +
:* ligation of exDirepeats in psB1C3 vector backbone and then transformation
 +
 
 +
:* colony-PCR, gel run, making cultures
 +
 
 +
:* miniprep of some of the 96 exDirepeats
 +
 
 +
<br>
 +
==  16/07 - 22/07 ==
 +
 
 +
:* transformation of synthesis products (Dnmt, hyperactive Gin, Gin L7C7, Tn3 and TAL-ORF) into DH10B-strain competent cells
 +
 
 +
:* amplification of psb1c3 vector backbone, then gel-run and gel-purification
 +
 
 +
:* picking of colonies (transformation of synthesis-products)
 +
 
 +
:* miniprep of synthesis-products
 +
 
 +
:* repeat of pcr-amplification of psb1c3 vector backbone
 +
 
 +
<br>
 +
== 30/07 - 05/08 ==
 +
 
 +
:* GGC to produce freiGEM-Mammo-Brick with CMV-promotor, Puromycin-resistance and postORF and TALEN-NG-vector backbone
 +
 
 +
:* to do so a extension-PCR on the parts was done
 +
 
 +
:* CMV-Promotor was taken out of iGEM Distribution Kit 2012
 +
 
 +
<br>
 +
==  06/08 - 12/08 ==
 +
 
 +
:* mutagenesis-PCR of pcb1c3 vector backbone to eliminate restriction site for BsmBI
 +
 
 +
:* repeat of GGC to get MammoBrick
 +
 
 +
:* gel-run of mutagenesis-PCR of psb1c3
 +
 
 +
<br>
 +
== 13/08 - 19/08 ==
 +
 
 +
:* repeating the assembly of MammoBrick vector containing CMV Promotor, PostORF-Part and Puromycin-ORF
 +
 
 +
:* repeating mutagenesis-PCR on vector backbone psb1c3
 +
 
 +
:* extPCR of TAL-ORF (synthesis-product) in order to produce a n-terminal kind of adapter to paste recombinase
 +
 
 +
:* producing an provisory mammalian expression vector --> cloning of TAL-ORF into mammalian vector backbone
 +
 
 +
:* to do so the vector and the insert have been digested and then ligated and transformed into dh10b e. coli strain bacteria
 +
 
 +
:* transformation of mutated vector backbone
 +
 
 +
:* colony pcr to test provisory mammalian expression vector
 +
 
 +
<br>
 +
== 20/08 - 26/08 ==
 +
 +
:* repeating mutagenesis pcr for vector backbone psb1c3 with another template
 +
 
 +
:* finding a new method for successful extension pcr and then digest and ligation into the psb1cr backbone
 +
 
 +
 
 +
<br>
 +
== 27/08 - 02/09 ==
 +
 
 +
:* finding out that CMV promotor taken out of the registry distribution kit is not good at all
 +
 
 +
:* trying to get another vector with cmv promotor and ordering new primer pair to amplify it
 +
 
 +
:* after finding a working method for direpeat extension, digestion and ligation into psb1c3 vector backbone we now started to execute it on our synthesized direpeats
 +
 
 +
 
 +
<br>
 +
== 03/09 - 09/09 ==
 +
 
 +
:* GGC-reaction in order to produce recombinase-linker-n-tal-orf construct
 +
 
 +
:* annealing of linker-part (was ordered as two single-strand primers)
 +
 
 +
:* after ggc-reaction was done a pcr-amplification on the new assembled part was executed
 +
 
 +
:* gel-run shows a very weak band at 2,7 kb for hyperactive gin recombinase
 +
 
 +
:* GGC-reaction in order to clone direpeats for a complete TAL-Domain into provisory mammalian expression vector
 +
 
 +
:* repeating the extextPCR on the recombinase-linker-n-tal-orf construct under different conditions after the first pcr reaction failed
 +
 
 +
:* amplification of mutated psb1c3 vector backbone
 +
 
 +
:* trying to clone Transcription Factor into provisory mammalian expression vector
 +
 
 +
:* repeating of GGC reaction in order to produce MammoBrick
 +
 +
:* still working on our toolkit, doing the final steps: sent them off for sequencing
 +
 
 +
<br>
 +
== 10/09 - 16/09 ==
 +
 
 +
:* doing the final steps in producing our toolkit: miniprep was done for the last three batches of direpeats, which can finally be sequenced on monday
 +
 
 +
:* we now have 75 successfully sequenced direpeats in the psb1c3 vector backbone, ready to send them off to igem headquarters
 +
 
 +
:* new working cmv promotor is now in psb1c3 vector backbone, too. we now have an improved, i.e. finally working, biobrick for the registry
-
{|align="justify"
 
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{{#calendar: title=Freiburg |year=2012 | month=05}}
 
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{{#calendar: title=Freiburg |year=2012 | month=06}}
 
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{{#calendar: title=Freiburg |year=2012 | month=07}}
 
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{{#calendar: title=Freiburg |year=2012 | month=08}}
 
-
{{#calendar: title=Freiburg |year=2012 | month=09}}
 
-
|}
 
-
{|align="center"
+
<br>
-
|[[Image:smallbarrev.png|960px|no frame]]
+
<br>
-
|}
+
<br>
 +
[[#top|Back to top]]

Latest revision as of 18:29, 24 October 2012




Notebook



NotebooksymbolT.png


04/06 - 10/06

  • Golden-Gate-Cloning-Reaction (GGC) to assemble a 12-repeat-TAL-TF, that recognizes the sequence TACATTGGACCTAT
  • transformation: GGC-reaction
  • making aliquots of ordered GGC-Primers (freiGEM-method)
  • making aliquots of ordered, i.e. synthesized, direpeats
  • extension-PCR of direpeats in order to produce diefferent restriction sites for correct location of direpeats
  • PCR-Purification of extension-PCR
  • mutagenesis-PCR of Zhang-plasmid to remove restriction sites (SpeI, PstI, EcoRI, XbaI) --> making the plasmid work with iGEM-standard


11/06 - 16/06

  • optimizing PCR conditions for extension of direpeats
  • redoing GGC-reaction
  • transformation of redone GGC-reaction
  • GGC á la freiGEM --> transformation
  • testing of iGEM-distribution kit


17/06 - 23/06

  • cloning of direpeats into pJET 1.2 vector-system
  • colony-PCR of freiGEM-GGC product
  • place sequencing order for freiGEM-GGC


24/06 - 01/07

  • optimizing of freiGEM-GGC under various conditions
  • transformation of pJET-direpeats into bacteria
  • using the iGEM distribution kit: Bba_A12564 (CMV+Luc) --> reporter-plasmid for DNA-methyl-transferase testing
  • Miniprep of GGC-transformation (1 successful)


02/07 - 08/07

  • extension-PCR with all 96 direpeats on one well-plate
  • transformation
  • PCR-amplification of all 4 iGEM-backbones --> testing different conditions
  • making bacteria competent for transformation


09/07 - 15/07

  • digest of exDirepeats with XbaI and PstI
  • nanodrop of exDirepeats
  • ligation of exDirepeats in psB1C3 vector backbone and then transformation
  • colony-PCR, gel run, making cultures
  • miniprep of some of the 96 exDirepeats


16/07 - 22/07

  • transformation of synthesis products (Dnmt, hyperactive Gin, Gin L7C7, Tn3 and TAL-ORF) into DH10B-strain competent cells
  • amplification of psb1c3 vector backbone, then gel-run and gel-purification
  • picking of colonies (transformation of synthesis-products)
  • miniprep of synthesis-products
  • repeat of pcr-amplification of psb1c3 vector backbone


30/07 - 05/08

  • GGC to produce freiGEM-Mammo-Brick with CMV-promotor, Puromycin-resistance and postORF and TALEN-NG-vector backbone
  • to do so a extension-PCR on the parts was done
  • CMV-Promotor was taken out of iGEM Distribution Kit 2012


06/08 - 12/08

  • mutagenesis-PCR of pcb1c3 vector backbone to eliminate restriction site for BsmBI
  • repeat of GGC to get MammoBrick
  • gel-run of mutagenesis-PCR of psb1c3


13/08 - 19/08

  • repeating the assembly of MammoBrick vector containing CMV Promotor, PostORF-Part and Puromycin-ORF
  • repeating mutagenesis-PCR on vector backbone psb1c3
  • extPCR of TAL-ORF (synthesis-product) in order to produce a n-terminal kind of adapter to paste recombinase
  • producing an provisory mammalian expression vector --> cloning of TAL-ORF into mammalian vector backbone
  • to do so the vector and the insert have been digested and then ligated and transformed into dh10b e. coli strain bacteria
  • transformation of mutated vector backbone
  • colony pcr to test provisory mammalian expression vector


20/08 - 26/08

  • repeating mutagenesis pcr for vector backbone psb1c3 with another template
  • finding a new method for successful extension pcr and then digest and ligation into the psb1cr backbone



27/08 - 02/09

  • finding out that CMV promotor taken out of the registry distribution kit is not good at all
  • trying to get another vector with cmv promotor and ordering new primer pair to amplify it
  • after finding a working method for direpeat extension, digestion and ligation into psb1c3 vector backbone we now started to execute it on our synthesized direpeats



03/09 - 09/09

  • GGC-reaction in order to produce recombinase-linker-n-tal-orf construct
  • annealing of linker-part (was ordered as two single-strand primers)
  • after ggc-reaction was done a pcr-amplification on the new assembled part was executed
  • gel-run shows a very weak band at 2,7 kb for hyperactive gin recombinase
  • GGC-reaction in order to clone direpeats for a complete TAL-Domain into provisory mammalian expression vector
  • repeating the extextPCR on the recombinase-linker-n-tal-orf construct under different conditions after the first pcr reaction failed
  • amplification of mutated psb1c3 vector backbone
  • trying to clone Transcription Factor into provisory mammalian expression vector
  • repeating of GGC reaction in order to produce MammoBrick
  • still working on our toolkit, doing the final steps: sent them off for sequencing


10/09 - 16/09

  • doing the final steps in producing our toolkit: miniprep was done for the last three batches of direpeats, which can finally be sequenced on monday
  • we now have 75 successfully sequenced direpeats in the psb1c3 vector backbone, ready to send them off to igem headquarters
  • new working cmv promotor is now in psb1c3 vector backbone, too. we now have an improved, i.e. finally working, biobrick for the registry





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