Team:Bilkent UNAM Turkey/Experiment

From 2011.igem.org

(Difference between revisions)

Revision as of 21:10, 21 September 2011

We ordered our genes. We optimized codon usage because of gene taken from E. cloacae.

Codon Usage Then we did restriction digestion and gel electrophoresis.
We repeat this step a lot because of failuire.I put right result

We used standard gel purification kit Our ligation style is really similar to iGEM's one.
Our one;

insert volume(µl):X

Cut Vector Volume(µl):X

DEPC-water(µl):8,5-2X

T4 DNA ligase(µl):0,5

Ligation Buffer(µl):1

Total Volume(µl):10

We transformed our plasmid into E.coli with a protocol.
We used invitrogen purification kit to get our plasmid. We sent genes to sequencing and sequencing data should be available on their link.

@@ Line 16: / Line 16: @@
 <br>We transformed our plasmid into E.coli with a <a href="http://www.med.nyu.edu/medicine/labs/blaserlab/Protocols/E-coli_competent_cells_protocol_&_transformation.pdf">protocol.</a><br>
 We used invitrogen <a href="http://tools.invitrogen.com/content/sfs/manuals/purelink_pro96_plasmid_kit_man.pdf">purification kit </a>to get our plasmid.
-We sent genes to sequencing and sequencing data shold be available on their <a href="http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2011&group=Bilkent_UNAM_Turkey">link</a>.
+We sent genes to sequencing and sequencing data should be available on their <a href="http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2011&group=Bilkent_UNAM_Turkey">link</a>.
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