Difference between revisions of "Part:BBa K1886008"
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<partinfo>BBa_K1886008 parameters</partinfo> | <partinfo>BBa_K1886008 parameters</partinfo> | ||
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+ | <h2>'''Characterization'''</h2> | ||
+ | <h3> BACKGROUND </h3> | ||
+ | <h4>Overview</h4> | ||
+ | Registered Parts in our wiki is the subunit of the entire AND Gate system, each of which has no function. So I will introduce our logical part of our project after the combination of all the subunits in the page of part [https://parts.igem.org/Part:BBa_K1886016 BBa_K1886016]. | ||
+ | <br><br> | ||
+ | <h3> Results </h3> | ||
+ | <h4>Gel electrophoretic analysis</h4> | ||
+ | [[File:K1886008.jpg|800px|thumb|left|Fig.1 Fig.1 Gel electrophoretic analyses of PCR products ]] |
Latest revision as of 02:53, 20 October 2016
AND GATE-output-1
This is a report system to test the AND GATE made up of SupD tRNA coding gene and T7 polymerase with two amber mutations. T7 promoter is a very specific promoter which is transcribed only by specific T7 RNA polymerase. Following the PT7 promoter is the reporter gene GFP, Only when the two inputs are given, the GFP gene can be expressed.
Sequence and Features
Assembly Compatibility:
- 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 693
Characterization
BACKGROUND
Overview
Registered Parts in our wiki is the subunit of the entire AND Gate system, each of which has no function. So I will introduce our logical part of our project after the combination of all the subunits in the page of part BBa_K1886016.