Coding
AID

Part:BBa_K103001:Design

Designed by: Michael Lower   Group: iGEM08_Warsaw   (2008-09-14)
Revision as of 13:00, 28 October 2008 by Smaegol (Talk | contribs) (→‎Design Notes)

AID protein


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 78
    Illegal SapI site found at 179


Design Notes

Preparation of BBa_K103001 is in details described [http://2008.igem.org/wiki/index.php?title=Team:Warsaw/JSTest&num=5&arg0=1_October_2008&arg1=6_October_2008&arg2=7_October_2008&arg3=8_October_2008&arg4=9_October_2008&name=Preparation%20of%20AID(BBa_K103001) here] (entries from Univeristy of Warsaw 2008 iGEM team notebook).

AID-coding fragment was amplified from [http://2008.igem.org/Wiki/Team:Warsaw/vectors/pMPM-T5-AID pMPM-T5-AID] vector using primers: 5' AAACTGCAGCGGCCGCTACTAGTAAAGCTTTCAAAGTCCCAAAGTACGAAATG 3' and 5' TATCTAGAACCATGGACAGCCTCTTG 3'. Resulting fragment was digested with XbaI and PstI and cloned into standard BioBrick vector (pSB1A3

Source

Human cDNA (plasmid Trc99a with AID from publication below)

References

Ref. [http://www.ncbi.nlm.nih.gov/pubmed/12097915?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum]