Difference between revisions of "Part:BBa K1602026"

 
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                 This part is capable of generating the <b> green fluorescent protein (GFP) </b> under the control of a T7 promotor while codon optimized for usage in <i>E.coli</i> (<a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>. Also the sequence of a Histag is fused to the gene sequence, improving the purification yield. Fusing the Si4-tag(<a href:"https://parts.igem.org/Part:BBa_K1028000">BBa_K1028000</a>) to the 3' end of the sequence, enables the proof of functional silica surface binding of the Si4tag.
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                 This part is capable of generating the <b> green fluorescent protein (GFP) </b> under the control of a T7 promotor while codon optimized for usage in <i>E.coli</i> (<a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>). Also the sequence of a Histag is fused to the gene sequence, improving the purification yield. Fusing the Si4-tag(<a href:"https://parts.igem.org/Part:BBa_K1028000">BBa_K1028000</a>) to the 3' end of the sequence, enables the proof of functional silica surface binding of the Si4tag.
 
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Latest revision as of 02:13, 19 September 2015

Inducible generator of HisTag-GFP_Si4-Tag fusion protein

This part is capable of generating the green fluorescent protein (GFP) under the control of a T7 promotor while codon optimized for usage in E.coli (BBa_B0034). Also the sequence of a Histag is fused to the gene sequence, improving the purification yield. Fusing the Si4-tag(BBa_K1028000) to the 3' end of the sequence, enables the proof of functional silica surface binding of the Si4tag.



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 BsaI.rc site found at 711