Difference between revisions of "Part:BBa K1144005"
Sylvita1015 (Talk | contribs) |
|||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1144005 short</partinfo> | <partinfo>BBa_K1144005 short</partinfo> | ||
Line 6: | Line 5: | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
+ | |||
+ | ===Characterization=== | ||
+ | |||
+ | To assess the strength of our GAL4 responsive promoter set (BBa_K1144001, BBa_K1144002, BBa_K1144003 and BBa_K1144004) when induced with Dexamethasone, we performed a fluorometric assay using mCherry as our reporter.Since we don't have our transactivating protein ready yet, we co-transformed our parts into the E. coli DH10B strain with the pAT7002 vector (Aoyama and Chua, 1997), which contains a well characterized Glucocorticoid Responsive Element that also uses the GAL4 DNA binding domain. | ||
+ | |||
+ | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 04:22, 28 September 2013
GAL4 activation reporter
The level of expression from the GAL1 promoter (Saccharomyces cerevisiae) is enhanced due to the presence of UAS sites. We fused pGAL1 with a KOZAC sequence, mCherry and the HHO1 yeast terminator to asses the level of expression due to the activacion of GAL4 binding domain
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 84
- 1000COMPATIBLE WITH RFC[1000]