Difference between revisions of "Part:BBa K1346011"
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[[File:ASG7-zoomed.png|900px]] | [[File:ASG7-zoomed.png|900px]] | ||
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+ | Compared to the other alpha factor responsive promoters, pASG7 has a high basal expression level, a sharply narrow range of expression, and a mid-level maximum output, comparable to pSAG1's maximum expression rate. | ||
[[File:140722_AFRP_GFP_DB_ROUND_4_zoomed.png|900px]] | [[File:140722_AFRP_GFP_DB_ROUND_4_zoomed.png|900px]] | ||
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− | [[File:AFRP_GFP_DB_ROUND_4_140722.png|900px]]<!-- Add more about the biology of this part here | + | [[File:AFRP_GFP_DB_ROUND_4_140722.png|900px]] |
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+ | Alpha factor responsive promoters were selected from the following paper: Roberts, Christopher J., et al (2000 Feb 4). Signaling and Circuitry of Multiple MAPK Pathways Revealed by a Matrix of Global Gene Expression Profiles. Science, 287(5454):873-80. http://www.ncbi.nlm.nih.gov/pubmed/10657304. | ||
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+ | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
Latest revision as of 21:26, 3 September 2014
pASG7
Promoter endogenous to s. cerevisiae that is induced by alpha factor. Characterized on flow cytometer by measuring its mean GFP fluorescence over 7 concentrations of alpha factor.
Compared to the other alpha factor responsive promoters, pASG7 has a high basal expression level, a sharply narrow range of expression, and a mid-level maximum output, comparable to pSAG1's maximum expression rate.
Alpha factor responsive promoters were selected from the following paper: Roberts, Christopher J., et al (2000 Feb 4). Signaling and Circuitry of Multiple MAPK Pathways Revealed by a Matrix of Global Gene Expression Profiles. Science, 287(5454):873-80. http://www.ncbi.nlm.nih.gov/pubmed/10657304.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 252
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 252
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 252
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 252
- 1000COMPATIBLE WITH RFC[1000]