Difference between revisions of "Part:BBa K1111012"

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<!--The expression of this plasmid was tested by transforming cells and looking for microscopy at either of a fluorescent antibody again streptavidin or a fluorescent biotin (biotin and streptavidin have a strong affinity, their Kd is 10-15 M).-->
 
<!--The expression of this plasmid was tested by transforming cells and looking for microscopy at either of a fluorescent antibody again streptavidin or a fluorescent biotin (biotin and streptavidin have a strong affinity, their Kd is 10-15 M).-->
  
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[[Image: Team-EPFL-Lausanne generalmap.jpg|thumb|250px|center|Figure 1: The Plasmid containing the constitutive promoter and superfolded GFP]]
 
  
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[[File:EPF-Lausanne map.jpg|400px|center|Figure : outline of the expected outcome of the plasmid]]
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[[File:EPF-Lausanne map.jpg||thumb|400px|center|Figure 1: outline of the expected outcome of the plasmid]]
  
 
==Usage and Biology==
 
==Usage and Biology==
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This part was designed to express streptavidin on the outer membrane of E.coli in order to attach biotinylated nanoparticles to the cells.   
 
This part was designed to express streptavidin on the outer membrane of E.coli in order to attach biotinylated nanoparticles to the cells.   
 
<br>Thus, it can be used in any experiment involving biotin-streptavidin affinity (attachment of cargo is one example, but we could also think of purification etc...).
 
<br>Thus, it can be used in any experiment involving biotin-streptavidin affinity (attachment of cargo is one example, but we could also think of purification etc...).
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==Datasheet==
 
==Datasheet==
 
For further Characterization, refer to the datasheet below.
 
For further Characterization, refer to the datasheet below.
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[[File:Team-EPF-Lausanne_Sheet1.jpg|thumb|270px|left|CharacterizationSheet Page1 ]]
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[[File: Team-EPF-Lausanne_Sheet2.jpg|thumb|270px|left|CharacterizationSheet Page2 ]]
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<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
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<br><br>[[File: Team-EPF-Lausanne_Sheet.pdf|thumb|270px|left|PDF link ]]
  
 
==<span class='h3bb'>Sequence and Features</span>==
 
==<span class='h3bb'>Sequence and Features</span>==

Latest revision as of 18:19, 4 October 2013

Ice Nucleation Protein fused to Streptavidin Alive

Introduction

It is a fusion protein between an Ice Nucleation Protein (INP) and Streptavidin Alive made by Gibson Assembly. INP is an outer membrane protein found in the genome of Pseudomonas syringae, that is recognized by the E.coli protein secretion machinery, and thus also exported in that organism.


Figure 1: outline of the expected outcome of the plasmid

Usage and Biology

This part was designed to express streptavidin on the outer membrane of E.coli in order to attach biotinylated nanoparticles to the cells.
Thus, it can be used in any experiment involving biotin-streptavidin affinity (attachment of cargo is one example, but we could also think of purification etc...).

Datasheet

For further Characterization, refer to the datasheet below.

CharacterizationSheet Page1
CharacterizationSheet Page2























File:Team-EPF-Lausanne Sheet.pdf

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 1727
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1649
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 1727
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 1727
    Illegal NgoMIV site found at 1036
    Illegal AgeI site found at 1691
    Illegal AgeI site found at 1742
  • 1000
    COMPATIBLE WITH RFC[1000]