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.
There is a problem with poping up if you see this note.