Difference between revisions of "Part:BBa K1022114"

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The construct is made by ligating the pT7 promoter [https://parts.igem.org/wiki/index.php?title=Part:BBa_I712074  BBa_I712074] in front of the lysis device from the biobrick [https://parts.igem.org/wiki/index.php?title=Part:BBa_K112808  BBa_K112808]. This is analyze how the lysis device can be controlled if needed.
 
The construct is made by ligating the pT7 promoter [https://parts.igem.org/wiki/index.php?title=Part:BBa_I712074  BBa_I712074] in front of the lysis device from the biobrick [https://parts.igem.org/wiki/index.php?title=Part:BBa_K112808  BBa_K112808]. This is analyze how the lysis device can be controlled if needed.
  
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[[Image:114.jpg|450px|center]]
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Description :
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The <i>E.coli</i> cells transformed with pT7 lysis cassette [https://parts.igem.org/wiki/index.php?title=Part:BBa_K1022114  BBa_K1022114] is grown on a plate reader which is capable of shaking and heating to 37˚C to take readings of the cells in exponential phase at every 10 minutes. Different range of IPTG concentration is used to characterize the bio – brick  [https://parts.igem.org/wiki/index.php?title=Part:BBa_K1022114  BBa_K1022114].  At time point, 160 minutes, IPTG is added according to the table below.
  
 
[[Image:Lysis TU Delft.jpg|450px|center]]
 
[[Image:Lysis TU Delft.jpg|450px|center]]
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Revision as of 09:43, 3 October 2013

pT7 : Lysis Device

This bio-brick codes for the promoter pT7(BBa_I712074) followed by the lysis device(BBa_K112808).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1404
    Illegal NheI site found at 1427
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1009
    Illegal AgeI site found at 1079
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 1660


Characterization

For more info, visit [http://2013.igem.org/Team:TU-Delft/Killswitch TU Delft iGEM13 Wiki !!]

The construct is made by ligating the pT7 promoter BBa_I712074 in front of the lysis device from the biobrick BBa_K112808. This is analyze how the lysis device can be controlled if needed.

114.jpg

Description : The E.coli cells transformed with pT7 lysis cassette BBa_K1022114 is grown on a plate reader which is capable of shaking and heating to 37˚C to take readings of the cells in exponential phase at every 10 minutes. Different range of IPTG concentration is used to characterize the bio – brick BBa_K1022114. At time point, 160 minutes, IPTG is added according to the table below.

Lysis TU Delft.jpg