After the O/N period, today we transformed the ligation finO+pSB1A3 into electrocompetent E. coli bacteria, strain DH10B. We followed protocol 3, without modifications (see Protocols section).
We then plated the transfomed cells in LB-AMP media, and let them grow at 37ºC for an O/N period.
finP+pSB1A3
We followed the same produce for the finP+pSB1A3 ligation.
Marcelo
YeastGuard
New biobrick in biobrick format
6 colonies of each new biobrick were chosen of the plates made yesterday to grow in liquid LB.
Then, we performed miniprep to get purified our new biobricks(Protocol 2).
We then digest the plasmids obtained by the miniprep with XbaI to confirm the correct ligation of the parts following the biobrick format (Protocolo x). However, the electrophoresis gel (down) showed a unexpected pattern of bands that can't confirm correctly ligations of our biobricks. =(
"
