Difference between revisions of "Part:BBa K3179102:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | pCMV-rtTA3 | + | This part consist with promoter pCMV can basic part rtTA3. pCMV is a strong mammalian expression promoter derived from human cytomegalovirus, usually used for routine expression, with high expression levels but may be inhibited in some cells. rtTA is a key component of Tet-On system, and rtTA3 is third generation rtTA. rtTA3 is an activation factor of pTRE. rtTA3 isn’t active when it is present alone, and it can be active when combine with doxycycline (DOX), then the complex can combine to pTRE and start the downstream transcription. When DOX get removed the rtTA3 will became no activation again. In our experiment, pCMV-rtTA3 is used to test the effect of the influence of different promoter to the expression of rtTA3. |
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===Source=== | ===Source=== |
Revision as of 22:46, 19 October 2019
pCMV-rtTA3
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part consist with promoter pCMV can basic part rtTA3. pCMV is a strong mammalian expression promoter derived from human cytomegalovirus, usually used for routine expression, with high expression levels but may be inhibited in some cells. rtTA is a key component of Tet-On system, and rtTA3 is third generation rtTA. rtTA3 is an activation factor of pTRE. rtTA3 isn’t active when it is present alone, and it can be active when combine with doxycycline (DOX), then the complex can combine to pTRE and start the downstream transcription. When DOX get removed the rtTA3 will became no activation again. In our experiment, pCMV-rtTA3 is used to test the effect of the influence of different promoter to the expression of rtTA3.
Source
pCMV-rtTA3