Difference between revisions of "Part:BBa K1442023:Design"
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<p> Lohmann V. et al. (1999). Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line. Science. 285 (5424), 110-113. </p> | <p> Lohmann V. et al. (1999). Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line. Science. 285 (5424), 110-113. </p> | ||
+ | <p> The exact sequence of the plasmid used in these experiments can be found on NCBI: http://www.ncbi.nlm.nih.gov/nuccore/5441831 </p> | ||
===References=== | ===References=== |
Latest revision as of 11:10, 6 October 2014
EMCV IRES
- 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
An AscI and BsrGI restriction site were added at the beginning and end of the sequence respectively in order to clone this part into our testing modules.
AscI is compatible with MluI
BsrGIis compatible with BsiWI and TatI
Source
This Internal Ribosome Entry Site (IRES) was derived from the Encephalomyocarditis Virus genome. It is commonly used in replicon experiments in HeLa cells. Specifically this sequence was taken from the detailed genome used in the Lohmann (1999) HCV replicon experiment.
Lohmann V. et al. (1999). Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line. Science. 285 (5424), 110-113.
The exact sequence of the plasmid used in these experiments can be found on NCBI: http://www.ncbi.nlm.nih.gov/nuccore/5441831
References
[1]Bochkov and Palmenberg, 2006, Translational efficiency of EMCV IRES in bicistronic vectors is dependent upon IRES sequence and gene location, BioTechniques, 41:283-292 (September 2006)
http://www.biotechniques.com/multimedia/archive/00002/BTN_A_000112243_O_2391a.pdf
[2]Lohmann V. et al. (1999). Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line. Science. 285 (5424), 110-113.
http://www.sciencemag.org/content/285/5424/110.long