Difference between revisions of "Part:BBa K103001:Design"
(→Design Notes) |
|||
(2 intermediate revisions by 2 users not shown) | |||
Line 9: | Line 9: | ||
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). | 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' | + | AID-coding fragment was amplified from [http://2008.igem.org/Wiki/Team:Warsaw/vectors/pMPM-T5-AID pMPM-T5-AID] vector using primers: 5' AAACTGCAGCGGCCGCTACTAGTATCAAAGTCCCAAAGTACGAAATG 3' and 5' TATCTAGAACCATGGACAGCCTCTTG 3'. Resulting fragment was digested with XbaI and PstI and cloned into standard BioBrick vector ([https://parts.igem.org/wiki/index.php?title=Part:pSB1A3 pSB1A3]) |
===Source=== | ===Source=== | ||
− | Human cDNA (plasmid | + | Human cDNA (plasmid pTrc99a with AID obtained from Svend Petersen-Mahrt, DNA Editing Laboratory, Cancer Research UK, Clare Hall Laboratories, South Mimms Hert EN6 3LD, United Kingdom) |
===References=== | ===References=== | ||
Ref. [http://www.ncbi.nlm.nih.gov/pubmed/12097915?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum] | Ref. [http://www.ncbi.nlm.nih.gov/pubmed/12097915?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum] |
Latest revision as of 13:59, 28 October 2008
AID protein
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE 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' AAACTGCAGCGGCCGCTACTAGTATCAAAGTCCCAAAGTACGAAATG 3' and 5' TATCTAGAACCATGGACAGCCTCTTG 3'. Resulting fragment was digested with XbaI and PstI and cloned into standard BioBrick vector (pSB1A3)
Source
Human cDNA (plasmid pTrc99a with AID obtained from Svend Petersen-Mahrt, DNA Editing Laboratory, Cancer Research UK, Clare Hall Laboratories, South Mimms Hert EN6 3LD, United Kingdom)
References
Ref. [http://www.ncbi.nlm.nih.gov/pubmed/12097915?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum]