Team:UANL Mty-Mexico/Notebook

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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>
<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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<caption align="bottom"><b>Figure 1.</b> Cloning strategy for contructions of fusion proteins.</caption>
<caption align="bottom"><b>Figure 1.</b> Cloning strategy for contructions of fusion proteins.</caption>
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Revision as of 03:41, 27 September 2012

iGEM UANL 2012


Notebook


Fusion proteins

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.




Figure 1. Cloning strategy for contructions of fusion proteins.



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