Difference between revisions of "Part:BBa K391007:Design"

(References)
(Design Notes)
 
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===Design Notes===
 
===Design Notes===
We designed forward and reverse primers with the appropriate standard BioBrick restriction sites (EcoRI, XbaI, SpeI, PstI) on each primer in order to put it on psb1C3.
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We designed forward and reverse primers with the appropriate standard BioBrick restriction sites (EcoRI, XbaI, SpeI, PstI) on each primer in order to put it on psb1c3.
One out of two sets of primers included a histidine tag, which would be used to isolate DspB after it is expressed.
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One out of two sets of primers included a histidine tag, which would be used to purify DspB after it is expressed.
 
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===Source===
 
===Source===

Latest revision as of 03:01, 28 October 2010

constitutive promoter-RBS-DspB (J23100:B0034:K391006)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1030
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We designed forward and reverse primers with the appropriate standard BioBrick restriction sites (EcoRI, XbaI, SpeI, PstI) on each primer in order to put it on psb1c3. One out of two sets of primers included a histidine tag, which would be used to purify DspB after it is expressed.

Source

The gene that encodes our protein, DspB, stems from the bacteria Actinobacillus actinomycetemcomitans.

References

1. Sigma Product Information for 4-Nitrophenyl N-acetyl-β-D-glucosaminide: [http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Product_Information_Sheet/2/n9376pis.Par.0001.File.tmp/n9376pis.pdf Product Information]