Device

Part:BBa_K2629000:Experience

Designed by: Elise Aubert   Group: iGEM18_Grenoble-Alpes   (2018-09-07)
Revision as of 14:03, 23 September 2018 by EliseMP (Talk | contribs)


Experiments were done on a plasmid in which the probe has been inserted, thanks the Gibson technic, in psB1C3-BBa_J04450.

Results of the clonning of the probe into psB1C3-BBa_J04450

Sequencage

Test A: Is this part able to detect the target for which it has been designed ?


mettre schema

Unfortunately, results were too heterogenous to bring any conclusions. Indeed, the number of colonies, for the 1:100 and 1:200 ratios, expected was not good enought (there is a possibility that the detector was badly digested and was consequently transformed).

Test B: Is this part able to detect specifically the target for which it has been designed ?


In order to evaluate the specificity of the detector part of BBa_K2629000, different “false target” sequences have been synthesized. An algorithm was made by iGEM Grenoble Alpes 2017 to give random sequences, more or less homologous to the original target with 5%, 15%, 25% and 50% randomly modified pairs of nucleotides (length is kept 36bp).
The algorithm can be found here :


T--grenoble-alpes--algo.png

Unfortunately, we did not have the opportunity and the time to carry out these experiments.

User Reviews

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