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Fok_a-Venu

Part:BBa_K243032

Designed by: Freiburg Bioware09   Group: iGEM09_Freiburg_bioware   (2009-10-20)
Revision as of 19:14, 21 October 2009 by Timo (Talk | contribs) (Detection)

Fok_a-Venus

This part is like part the protein domain Fok_a from our universal endonuclease, but it has an additional linked YFP-marker.

Usage and Biology

The addition of a fluorescent protein(Venus) to the protein construct, enables the detection by fluorescence microscope and new way of purification by GFP-trap column.The Venus protein was fusioned C'terminal to the protein domain, so when the protein is expressed the fluorescence signal of the Venus protein can be seen.

Detection

There was a strong fluorescence signal under the fluorescence microscope after the induction of the cells with IPTG.The E.colis(RV308) were excited with the wavelength 505nm and then some pictures of the fluorescencewere made.
Freiburg RV308 mit fluo Oligos3 (c1+c2).JPG

The cell extract were check by SDS-page to get information about the expression of proteins.
SDSfokvenus.jpg SDS gel; pEx Venus-Fok_a in BL21de3; lanes: Marker (ColorPlus Prestained Protein Marker, Broad Range), clone 1 uninduced, clone 1 induced, clone 1 induced, clone 2 uninduced, clone 2 induced, control (His-FluA-SplitLi-Fok_i + His-Dig-SplitLi-Fok_a) uninduced, control induced)----

Purification

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 487


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