Glasgow/Wetlab

From 2007.igem.org

< Glasgow(Difference between revisions)
 
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*'''''First selection of biobricks transformed.'''
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*'''First selection of biobricks transformed.'''
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*'''''Preparation of stocks.'''
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*'''Preparation of stocks.'''
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*'''''Researched DmpR, XylR and DntR sensor systems.'''
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*'''Researched DmpR, XylR and DntR sensor systems.'''
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*'''''Designed primers for DmpR, DntR, XylR and associated promoters.'''
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*'''Designed primers for DmpR, DntR, XylR and associated promoters.'''
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*'''phzD→phzG successfully cloned into TOPO vector.'''
*'''phzD→phzG successfully cloned into TOPO vector.'''
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*'''''Contains further work achieved.'''''
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*'''Contains further work achieved.'''
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*'''''XylR and Pr cloned into construction vectors.'''''
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*'''XylR and Pr cloned into construction vectors.'''
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*'''''XylR and Pr put next to responsive promoter and luciferase.'''''
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*'''XylR and Pr put next to responsive promoter and luciferase.'''
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Latest revision as of 11:54, 26 October 2007

Uog.jpg Back To
Glasgow's
Main Page 		Go To
Glasgow's
Modelling Page
Protocols References Resources Sequences Biobricks
Used 		Gels

Click on a week number for more detailed lab book...


Week 1
Week 2
  • First selection of biobricks transformed.
  • Preparation of stocks.
  • Researched DmpR, XylR and DntR sensor systems.
  • Designed primers for DmpR, DntR, XylR and associated promoters.
Week 3
Week 4
  • BioBricks tested by digestion and PCR.
  • PCR with new primers associated with DntR and XylR.
  • phzM and phzS cloned into TOPO vectors.
  • Primer design for 7 gene operon.
  • DntR cloned into TOPO vector.
  • Primer design for XylR and associated genes.
  • Death gene cloned into TOPO vector.
  • Primer design for death gene.
Week 5
Week 6
  • Suspected amplification of 7 gene operon.
  • phzM and phzS confirmed as present in TOPO vectors.
  • Confirmed presence of death gene plasmid in some vectors.
  • Miller assay performed with DntR system.
  • Yeast cells.
  • Biobricks made of phzM, phzS, and DntR.
Week 7
Week 8
  • Utilised new biobricks.
  • Site directed mutagenesis of phzM completed.
  • Site directed mutagenesis of phzS completed.


Week 9
Week 10+
  • phzD→phzG successfully cloned into TOPO vector.
  • Contains further work achieved.
  • XylR and Pr cloned into construction vectors.
  • XylR and Pr put next to responsive promoter and luciferase.
Protocols References Resources Orders Biobricks
Used 		Gels
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