Difference between revisions of "Part:BBa K2387003"
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===Functional Parameters===
 
===Functional Parameters===
  
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In order to test the functionality of this protein under the araC/pBad promoter, the absorbance and the fluorescence spectra were measured after induction with 0.002% arabinose (Figure 1).  
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In order to test the functionality of this protein under the araC/pBad promoter, the absorbance and the fluorescence spectra were measured after induction with 0.2% arabinose (Figure 1).  
  
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[[file:T--Wageningen_UR--eYFP.jpg|400px|center|thumb|<p align="justify">'''Figure 1: Absorbance and fluorescence spectra of eYFP, measured after induction with 0.002% arabinose.'''</p>]]
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[[file:T--Wageningen_UR--eYFP.jpg|400px|center|thumb|<p align="justify">'''Figure 1: Absorbance and fluorescence spectra of eYFP, measured after induction with 0.2% arabinose.'''</p>]]
  
 
This protein is part of a collection of split proteins developed for BiFC analysis and tested with the CpxR system ([https://parts.igem.org/Part:BBa_K2387032 BBa_K2387032]). These proteins were characterized through multiple experiments using as interacting proteins antiparallel synthetic leucine zippers. The proteins of this collection are the ones found in Table 1.  
 
This protein is part of a collection of split proteins developed for BiFC analysis and tested with the CpxR system ([https://parts.igem.org/Part:BBa_K2387032 BBa_K2387032]). These proteins were characterized through multiple experiments using as interacting proteins antiparallel synthetic leucine zippers. The proteins of this collection are the ones found in Table 1.  

Revision as of 11:19, 31 October 2017


eYFP controlled by inducible araC/pBAD promoter

Fluorescent protein eYFP is put under the control of the L-arabinose inducible araC/pBAD promoter. Strong RBS BBa_B0034 is used to regulate transcription.

It is used as to control the functioning of inducible promoter araC/pBAD.

T--Wageningen_UR--araCpBAD_test.png

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961


Functional Parameters

In order to test the functionality of this protein under the araC/pBad promoter, the absorbance and the fluorescence spectra were measured after induction with 0.2% arabinose (Figure 1).

Figure 1: Absorbance and fluorescence spectra of eYFP, measured after induction with 0.2% arabinose.

This protein is part of a collection of split proteins developed for BiFC analysis and tested with the CpxR system (BBa_K2387032). These proteins were characterized through multiple experiments using as interacting proteins antiparallel synthetic leucine zippers. The proteins of this collection are the ones found in Table 1.

Table 1: Split Proteins.
Protein Part Number (Full length) Part Number (Split Protein)
mRFP BBa_K2387054 BBa_K2387055
eYFP BBa_K2387003 BBa_K2387065
mVenus BBa_K2387045 BBa_K2387046
sfGFP BBa_K2387047 BBa_K2387048
mCerulean BBa_K2387052 BBa_K2387053