Difference between revisions of "Part:BBa K898890:Design"
Line 13: Line 13:
  
 
<center>
 
<center>
−
https://static.igem.org/mediawiki/2012/5/50/YFPFluorescence.png</center>
+
[[Image:https://static.igem.org/mediawiki/2012/5/50/YFPFluorescence.png width=100%]]
 +
 
 +
</center>
  
 
With regards to our hypothetical results, our experimental fluorescence measurements were substantially faithful to our predictions. Looking at columns 5, 6, 7, and 8, our observations appear to be in line with what we have predicted in introducing the wild type PUF-PIN to constructs containing a control recognition site and a specific recognition site. Columns 1 and 2 are negative fluorescence controls while Columns 3 and 4 are positive fluorescence controls measured without the influence of any sort of binding site.
 
With regards to our hypothetical results, our experimental fluorescence measurements were substantially faithful to our predictions. Looking at columns 5, 6, 7, and 8, our observations appear to be in line with what we have predicted in introducing the wild type PUF-PIN to constructs containing a control recognition site and a specific recognition site. Columns 1 and 2 are negative fluorescence controls while Columns 3 and 4 are positive fluorescence controls measured without the influence of any sort of binding site.

Revision as of 03:46, 4 October 2012

wtPUF+PIN


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 1297
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 35
  • 1000
    COMPATIBLE WITH RFC[1000]


Characterization Method

PUFPINreporter.png


This figure includes the resulting PUF-PIN proteins interacting with the binding sites. The wild type binding site placed in between RBS and YFP, is represented by the orange oval. The yellow rounded rectangle represents the YFP reporter gene.

File:Https://static.igem.org/mediawiki/2012/5/50/YFPFluorescence.png width=100%

With regards to our hypothetical results, our experimental fluorescence measurements were substantially faithful to our predictions. Looking at columns 5, 6, 7, and 8, our observations appear to be in line with what we have predicted in introducing the wild type PUF-PIN to constructs containing a control recognition site and a specific recognition site. Columns 1 and 2 are negative fluorescence controls while Columns 3 and 4 are positive fluorescence controls measured without the influence of any sort of binding site.

Source

The PUF domain from human Pum1 (residue 828-1176) and the PIN domain from human Smg6 (residue 1238-1421)

References

Professor Zefeng Wang, University of North Carolina- Chapel Hill

http://www.med.unc.edu/pharm/people/primaryfaculty/zefeng-wang/wang