Difference between revisions of "Part:BBa K3453101:Design"

 
 
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===Design Notes===
 
===Design Notes===
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Golden Gate (BsaI) adapter ([[Part:BBa_K3453001|BBa_K3453001]]) + sfGFP-LVAtag ([[Part:BBa_K2675006|BBa_K2675006]]) +SBa_000587 Terminator ([[Part:BBa_K3453000|BBa_K3453000]]).
+
Golden Gate (BsaI) adapter ([[Part:BBa_K3453001|BBa_K3453001]]) + sfGFP-LVAtag ([[Part:BBa_K2675006|BBa_K2675006]]) + SBa_000587 Terminator ([[Part:BBa_K3453000|BBa_K3453000]]).
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+
−
 
+
  
 
===Source===
 
===Source===
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===References===
 
===References===
 +
[1] Engler C, Kandzia R, Marillonnet S. A one pot, one step, precision cloning method with high throughput capability. PLoS One (2008) 3, e3647.
 +
 +
[2] Engler C, Gruetzner R, Kandzia R, Marillonnet S. Golden gate shuffling: a one-pot DNA shuffling method based on type IIs restriction enzymes. PLoS One (2009) 4, e5553.
 +
 +
[3] Pédelacq JD, Cabantous S, Tran T, Terwilliger TC, Waldo GS. Engineering and characterization of a superfolder green fluorescent protein. Nat Biotechnol (2006) 24, 79-88.
 +
 +
[4] Purcell O, Grierson CS, Bernardo Md, Savery NJ. Temperature dependence of ssrA-tag mediated protein degradation. J Biol Eng (2012) 6, 10.
 +
 +
[5] Temme K, Hill R, Segall-Shapiro TH, Moser F, Voigt CA. Modular control of multiple pathways using engineered orthogonal T7 polymerases. Nucleic Acids Res (2012) 40, 8773-8781.

Latest revision as of 17:06, 3 October 2020


Golden Gate (BsaI) adapter + sfGFP-LVAtag + SBa_000587 terminator


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 8
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 45
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 14
    Illegal BsaI.rc site found at 2


Design Notes

Golden Gate (BsaI) adapter (BBa_K3453001) + sfGFP-LVAtag (BBa_K2675006) + SBa_000587 Terminator (BBa_K3453000).

Source

DNA synthesis

References

[1] Engler C, Kandzia R, Marillonnet S. A one pot, one step, precision cloning method with high throughput capability. PLoS One (2008) 3, e3647.

[2] Engler C, Gruetzner R, Kandzia R, Marillonnet S. Golden gate shuffling: a one-pot DNA shuffling method based on type IIs restriction enzymes. PLoS One (2009) 4, e5553.

[3] Pédelacq JD, Cabantous S, Tran T, Terwilliger TC, Waldo GS. Engineering and characterization of a superfolder green fluorescent protein. Nat Biotechnol (2006) 24, 79-88.

[4] Purcell O, Grierson CS, Bernardo Md, Savery NJ. Temperature dependence of ssrA-tag mediated protein degradation. J Biol Eng (2012) 6, 10.

[5] Temme K, Hill R, Segall-Shapiro TH, Moser F, Voigt CA. Modular control of multiple pathways using engineered orthogonal T7 polymerases. Nucleic Acids Res (2012) 40, 8773-8781.