Outline: Experiments 12a-12b
1. Plasmid Minipreparation of pAMP/pKAN Recombinants
Obtain your two tubes of overnight culture from the shaking waterbath. Label two eppendorf tubes "M1" and "M2". Keep your two samples separate throughout the procedure, and remember if you are isolating pAMP, pKAN, or pLIG (the potential recombinant).
Make the following changes in the protocol for Experiment 12a (minipreparation). The rest of the protocol will be the same as the lab manual:
A) Use a P1000 to transfer all of the overnight culture to the eppy tube. Don't worry if there is less than 1 ml. Put the glass test tubes on a rack by the sink and remove the tape and the cap. Give them a squirt of 30% bleach and leave them on the rack to soak.
B) For step #11, it is very
important to avoid all the white cell debris or it will
inhibit
the restriction digest. Use a P200 to draw up the 400 ul
of supernatant, and wipe off the tip with a small piece of Kimwipe
before
transferring to a clean eppy tube.
Make sure the supernatant is completely
free of particles. Spin and transfer a second time if you can see
small
pieces floating in the tube.
C) Remember that step #12 is a carefully-timed step.
D) At step #20, add 30 ul
of TE to your DNA pellet instead of
the
15 ul stated
in
the lab manual.
2. Restriction Analysis of Purified pAMP/pKAN Recombinants
Set up restriction digests:
Use a permanent marker to label four eppy tubes. Use
the table below as a checklist when adding reagents.
| Tube | M1 | M2 |
+RNAse |
H2O | HindIII | BamHI |
| M1(-) | 10 ul |
|
6 ul |
|
|
|
| M2(-) | 10 ul |
|
6 ul |
|
|
|
| M1(+) | 10 ul |
|
4 ul |
|
|
|
| M2(+) | 10 ul |
|
4 ul |
|
|
When it is time to load the gel, add 4 ul of 6x tracking dye to each tube. Load 20 ul of each sample. We will have separate gels for the pAMP, pKAN, and pLIG miniprep samples.
Dr. Chapman will load the controls: undigested and
digested
pAMP, undigested and digested pKAN, and Lambda HindIII digest.