Difference between revisions of "Part:BBa K1150044"

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===Usage and Biology===
 
===Usage and Biology===
Fusion of [https://parts.igem.org/Part:BBa_K1150041 Target 3] and [https://parts.igem.org/Part:BBa_K1150042 Target 4].
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Fusion of [https://parts.igem.org/Part:BBa_K1150041 bla-target 3] and [https://parts.igem.org/Part:BBa_K1150042 bla-target 4].
 
This RNAimer was build via iGEM-ligation method and contains the DNA-target sequences of two areas of the bla-gene. This enables multiple gene targeting throught one plasmid. The transfection with such a multiple target-plasmid avoids additional cell stress compared to transfection with serveral single target-plasmids.   
 
This RNAimer was build via iGEM-ligation method and contains the DNA-target sequences of two areas of the bla-gene. This enables multiple gene targeting throught one plasmid. The transfection with such a multiple target-plasmid avoids additional cell stress compared to transfection with serveral single target-plasmids.   
  

Revision as of 13:19, 2 October 2013

uniCAS RNaimer multiple targets to Bla target 3 and 4

uniCAS RNaimer multiple targets to Bla target 3 and 4
Function twofold targeting of the bla-gen with one plasmid
Use in Mammalian cells
RFC standard RFC 25
Backbone pSB1C3
Submitted by [http://2013.igem.org/Team:Freiburg Freiburg 2013]

Usage and Biology

Fusion of bla-target 3 and bla-target 4. This RNAimer was build via iGEM-ligation method and contains the DNA-target sequences of two areas of the bla-gene. This enables multiple gene targeting throught one plasmid. The transfection with such a multiple target-plasmid avoids additional cell stress compared to transfection with serveral single target-plasmids.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 224
    Illegal BglII site found at 1061
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 216
    Illegal BsaI.rc site found at 1053