Composite

Part:BBa_K3352008

Designed by: Tsuyoshi Misaki   Group: iGEM20_TAS_Taipei   (2020-10-18)
Revision as of 16:43, 18 October 2020 by Registry (Talk | contribs)

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T7 + New RBS & Terminator + SplintR Ligase Expressing Construct

Construct Design

We improved this construct by using pET3a vectors with appropriate BioBrick prefixes and suffixes that fulfill the assembly standard. pET vectors include the T7 bacteriophage gene 10, which promotes high-level transcription and translation. Utilizing both a T7 promoter, T7 terminator, and an extended UTR sequence around the RBS and before the terminator, we would maximize the protein expression for our enzymes.

Characterization

Our SDS-PAGE results show that both purified proteins migrate at the expected sizes. However, due to the presence of unfavorable buffer conditions in our eluted proteins, we performed a buffer exchange to reach the desired pH and storage conditions for our enzymes. We used these proteins for our viral detection test.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1029
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 869
  • 1000
    COMPATIBLE WITH RFC[1000]


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Categories
Parameters
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