Difference between revisions of "IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/09/10"

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(Floor Two)
(Floor One)
 
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==Floor One==
 
==Floor One==
 
The results from the 16S sequences returned. The DNA sequences were run through BLAST to find matching sequences in the database ''table 1''.
 
The results from the 16S sequences returned. The DNA sequences were run through BLAST to find matching sequences in the database ''table 1''.
[[Image:Example.jpg]]
 
  
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Table 1: The strains of samples 1, 5, 7, 8 and 10 found using BLAST analysis.
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[[Image:Graph.png]]
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==Floor Two==
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Colonies 2-4 from the plate transformed with BL21 cells containing pET28AntA and AntGRFP plasmids(16/08) were used to inoculate three fresh 10ml LB with added Kanamycin and Chlorophenicol. They were incubated overnight at 37°C with shaking.
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__NOTOC__
  
 
==Floor Two==
 
==Floor Two==

Latest revision as of 16:03, 29 September 2013

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Floor One

The results from the 16S sequences returned. The DNA sequences were run through BLAST to find matching sequences in the database table 1.

Table 1: The strains of samples 1, 5, 7, 8 and 10 found using BLAST analysis. Graph.png

Floor Two

Colonies 2-4 from the plate transformed with BL21 cells containing pET28AntA and AntGRFP plasmids(16/08) were used to inoculate three fresh 10ml LB with added Kanamycin and Chlorophenicol. They were incubated overnight at 37°C with shaking.




Floor Two

Colonies 2-4 from the plate transformed with BL21 cells containing pET28AntA and AntGRFP plasmids(16/08) were used to inoculate three fresh 10ml LB with added Kanamycin and Chlorophenicol. They were incubated overnight at 37°C with shaking.


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