Difference between revisions of "Part:BBa K1433012:Experience"
| Line 1: | Line 1: | ||
| − | |||
__NOTOC__ | __NOTOC__ | ||
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter | This experience page is provided so that any user may enter their experience using this part.<BR>Please enter | ||
| Line 5: | Line 4: | ||
===Applications of BBa_K1433012=== | ===Applications of BBa_K1433012=== | ||
| + | |||
| + | |||
| + | ===Xis-Mediated attL/R Inversion Assay=== | ||
| + | <p>AttB/P flanking region inversion only counts for half of the reversible switch; Xis-mediated inversion is the other important part of the switch. Only when the two parts work, these bistable switch can be controlled to turn on and off downstream genes.</p> | ||
| + | [[File:ZJU_reset.png|820px|thumb|center|'''Fig. 1.''' RFP and qRT-PCR promoter analyses.]] | ||
| + | |||
| + | <p>In case of the cytotoxicity of Xis and system chaos caused by constitutive expression of Xis, we put Xis CDS downstream of a L-arabinosed promoter, PBad. We constructed another plasmid called Reset and co-transform it with Int-6N to attest the inversion after Xis expresses.</p> | ||
| + | <p>Under the Arabinose concentration of 50mM, partial inversion from RFP to GFP was observed. Unfortunately, we don’t have enough time to tune the Xis expression relative to Int expression as what we do in the RBS modulation experiment.</p> | ||
| + | |||
| + | |||
===User Reviews=== | ===User Reviews=== | ||
Latest revision as of 23:24, 17 October 2014
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K1433012
Xis-Mediated attL/R Inversion Assay
AttB/P flanking region inversion only counts for half of the reversible switch; Xis-mediated inversion is the other important part of the switch. Only when the two parts work, these bistable switch can be controlled to turn on and off downstream genes.
In case of the cytotoxicity of Xis and system chaos caused by constitutive expression of Xis, we put Xis CDS downstream of a L-arabinosed promoter, PBad. We constructed another plasmid called Reset and co-transform it with Int-6N to attest the inversion after Xis expresses.
Under the Arabinose concentration of 50mM, partial inversion from RFP to GFP was observed. Unfortunately, we don’t have enough time to tune the Xis expression relative to Int expression as what we do in the RBS modulation experiment.
User Reviews
UNIQc28b7a2bcd0b45e0-partinfo-00000000-QINU UNIQc28b7a2bcd0b45e0-partinfo-00000001-QINU