Team:UANL Mty-Mexico/Notebook

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<p><br><h3>Notebook</h3><br></p>
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<p><br><h3>Cloning Strategy</h3><br></p>
<p><b>Fusion proteins</b></p>
<p><b>Fusion proteins</b></p>
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<p>We used a cloning strategy similar to the Standard Assembly 21 based on the compatible restriction sites BglII and BamHI. A scar is obtained which translated result in the benefical aminoacids glicine and serine (Figure 1). In contrast with the Standar Assembly 21, the XhoI site was replaced with a SpeI site, which allow us to use the Standard Assembly 10 backbones.</p>
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<p>We used a cloning strategy similar to the Standard Assembly 21, based on the compatible restriction sites BglII and BamHI. Briefly, a scar is obtained which translation results in the benefical amino acids glicine and serine (Figure 1). In contrast with the Standar Assembly 21, the XhoI site was replaced with a SpeI site, which allows us to use the Standard Assembly 10 backbones.</p>
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Revision as of 03:44, 27 September 2012

iGEM UANL 2012


Cloning Strategy


Fusion proteins

We used a cloning strategy similar to the Standard Assembly 21, based on the compatible restriction sites BglII and BamHI. Briefly, a scar is obtained which translation results in the benefical amino acids glicine and serine (Figure 1). In contrast with the Standar Assembly 21, the XhoI site was replaced with a SpeI site, which allows us to use the Standard Assembly 10 backbones.




Figure 1. Cloning strategy for contructions of fusion proteins.



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