Difference between revisions of "Part:BBa M50050:Experience"
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===Conclusions=== | ===Conclusions=== | ||
| + | ====Western Blot==== | ||
| + | Based on our analysis of our Western blot, we concluded that we were successful in transfecting our E. coli strain with the correct plasmid and gene sequence. For BBa_M50050, we looked at well sections A and B (BBa_M50050 transfected E. coli at 0 μM and 1000 μM in-solution concentration respectively) compared to the wild-type controls (C and F). What we see is that there are bands of proteins located at the 40 kilodaltons (the anticipated length) in sections A and B, but not in the control sections C and F. | ||
===User Reviews=== | ===User Reviews=== | ||
Revision as of 17:35, 11 December 2016
Applications of BBa_M50050
- Standardized growth control for bacteria species that have pathways for sensing and responding to Autoinducer-2.
Stanford Location
Plasmid Name: LuxS Synthase Plasmid
DNA 2.0 Gene #: pD441-CH
Organism: E. coli
Device Type: Actuator
Glycerol Stock Barcode: 0133027189
Box Label: BIOE44 F16
Data
Conclusions
Western Blot
Based on our analysis of our Western blot, we concluded that we were successful in transfecting our E. coli strain with the correct plasmid and gene sequence. For BBa_M50050, we looked at well sections A and B (BBa_M50050 transfected E. coli at 0 μM and 1000 μM in-solution concentration respectively) compared to the wild-type controls (C and F). What we see is that there are bands of proteins located at the 40 kilodaltons (the anticipated length) in sections A and B, but not in the control sections C and F.
User Reviews
UNIQ2e519902d98b8305-partinfo-00000000-QINU UNIQ2e519902d98b8305-partinfo-00000001-QINU