Difference between revisions of "Part:BBa K404101"
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__NOTOC__
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<partinfo>BBa_K404101 short</partinfo> <br/>
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{| style="color:black" cellpadding="6" cellspacing="1" border="2" align="left"
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! colspan="2" style="background:#66bbff;"|[https://parts.igem.org/Part:BBa_K404101[AAV2]-right-ITR]
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|-
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|'''BioBrick Nr.'''
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|[https://parts.igem.org/Part:BBa_K404101 BBa_K404101]
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|-
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|'''RFC standard'''
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|[https://parts.igem.org/Help:Assembly_standard_10 RFC 10]
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|-
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|'''Requirement'''
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|pSB1C3<br>
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|-
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|'''Source'''
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|pAAV_MCS provided by Stratagene
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|-
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|'''Submitted by'''
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|[http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]
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|}
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<br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br />
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This BioBrick is a very GC-rich sequence with several palindromic motifs, which form strong hairpin structures. By using the Virus Construction Kit of the Freiburg iGEM team 2010, any gene of interest, which is cloned between this part and the left ITR can be packaged into the AAV2 capsid. These recombinant AAV2 particles can be used for  different applications, and were mainly created for therapeutic usage, including cancer treatment with prodrug activating enzymes or imaging approaches.  
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Usage and Biology<br/>
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The AAV2 ITRs serve as primers for the host cells’ DNA polymerase which converts the single-stranded virus genome into double-stranded DNA as a part of the viruses replicative cycle. They also play important roles in the virus integration into and rescue from the hosts genome, the formation of concatamers in the host cell nucleus and the encapsidation of the viral genome(K. Berns 1990). Due to these essential functions, the ITR structures cannot be deleted from a viral vector and need to be delivered in cis.
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[[Image:Freiburg10_VectorplasmidBricks 2.png|thumb|center|480px]]<br>
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<!-- Add more about the biology of this part here
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===Usage and Biology===
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<!-- -->
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K404101 SequenceAndFeatures</partinfo>
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<!-- Uncomment this to enable Functional Parameter display
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===Functional Parameters===
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<partinfo>BBa_K404101 parameters</partinfo>
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<!-- -->

Latest revision as of 16:17, 10 May 2013

[AAV2]-right-ITR

[AAV2-right-ITR]
BioBrick Nr. BBa_K404101
RFC standard RFC 10
Requirement pSB1C3
Source pAAV_MCS provided by Stratagene
Submitted by [http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]















This BioBrick is a very GC-rich sequence with several palindromic motifs, which form strong hairpin structures. By using the Virus Construction Kit of the Freiburg iGEM team 2010, any gene of interest, which is cloned between this part and the left ITR can be packaged into the AAV2 capsid. These recombinant AAV2 particles can be used for different applications, and were mainly created for therapeutic usage, including cancer treatment with prodrug activating enzymes or imaging approaches.


Usage and Biology

The AAV2 ITRs serve as primers for the host cells’ DNA polymerase which converts the single-stranded virus genome into double-stranded DNA as a part of the viruses replicative cycle. They also play important roles in the virus integration into and rescue from the hosts genome, the formation of concatamers in the host cell nucleus and the encapsidation of the viral genome(K. Berns 1990). Due to these essential functions, the ITR structures cannot be deleted from a viral vector and need to be delivered in cis.


Freiburg10 VectorplasmidBricks 2.png

Sequence and Features


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
    COMPATIBLE WITH RFC[1000]