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Team:UANL Mty-Mexico/Wet lab/Constructions
From 2011.igem.org
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Other methodologies were followed, as mention in the section <a href = "https://2011.igem.org/Team:UANL_Mty-Mexico/Wet_lab/Photocassette">Photocassette Construction</a>, using PCR for cloning. | Other methodologies were followed, as mention in the section <a href = "https://2011.igem.org/Team:UANL_Mty-Mexico/Wet_lab/Photocassette">Photocassette Construction</a>, using PCR for cloning. | ||
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| + | Both methodologies were performed while doing classic BioBrick Assembly. | ||
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Revision as of 05:00, 29 September 2011
Construction of whole circuits for this project was planed as detailed in the next three figures. Briefly, it consisted on joining CDS to RBS and terminator in the first stage, this for constructing almost complete genes. This constructions would allow combination of multiple joint to different promoters that would be in the next stage, which includes gene construction. For the last stage, genes would be combine in different orders to make complete circuits.
Note: Original idea for circuit was planed to be regulated through chemical inputs or light induction systems. That is why multiple promoters were added.
For construction of this circuit, different approaches were planed. One of them consisted on joining three parts at a time, reducing number of cloning steps as shown previously.
Other methodologies were followed, as mention in the section Photocassette Construction, using PCR for cloning.
Both methodologies were performed while doing classic BioBrick Assembly.
