Difference between revisions of "BISC209: Lab7"

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=='''PCR CLEAN UP with EXOSAPit'''==
We will have to clean up our reactions for sequencing to remove the excess dNTPS, primers, and pcr product contaminants using EXOSAP it. <BR><BR>
When PCR amplification is complete, any unconsumed dNTPs and primers remaining in the PCR product mixture will interfere with these methods. ExoSAP-IT removes these contaminants.
ExoSAP-IT contains two hydrolytic enzymes, Exonuclease I and Shrimp Alkaline Phosphatase, together in a proprietary buffer. It removes unwanted dNTPs and primers from PCR products. Exonuclease I removes residual single-stranded primers and any extraneous single-stranded DNA produced in the PCR. Shrimp Alkaline Phosphatase removes the remaining dNTPs from the PCR mixture.<BR<BR>
For those pcr reactions that resulted in a single product of the expected size, combine 1.5 microliters of your pcr reaction with 3.5 microliters of EXOSAPIT master mix in clearly labeled pcr tube of your team color. Place those tubes in the thermal cycler and record the position of each of your samples on the 96 well sheet provided. For any amplifications that were not successful or resulted in multiple fragments of the wrong size, consult with your instructor about whether or not to include them. <BR><BR>
The PCR program will be: 37C for 30 min. and 80C for 15 min. (to denature the enzymes). We will use 3 microliters of the ExoSapit reaction for sequencing.<BR><BR>
=='''Agarose Gel Electrophoresis of PCR products'''==
=='''Agarose Gel Electrophoresis of PCR products'''==

Revision as of 11:10, 13 January 2010

Wellesley College-BISC 209 Microbiology -Spring 2010

Agarose Gel Electrophoresis of PCR products

DNA is uniformly negatively charged and will,therefore, move toward the positive electrode. The separation is determined by the size or mass of the molecule or fragments of DNA.

BISC110 gel2.jpg

You will run your cleaned-up pcr products on a gel of 1.0 to 1.2% SeakemLE agarose solution (w/v) in 0.5x TBE buffer with Sybr Green stain to assess your success at amplifying 16s rDNA from each of your soil bacteria that you want to identify.

Keep your pcr products on ice until your instructor tells you that the gel is ready to load.
1. Pipet 1μL of loading dye for each of your pcr products on a piece of parafilm (use a P10 and space out the drops so they are not near each other). You should have 5 pcr products per person: 4 bacteria to id and one neg (water) control.
2. Using a new tip, pipet 5μL of a pcr product into one of the drops of loading dye, mix with the pipet tip and then draw up all of it and dispense it into a well of the gel.
3. Fill out the gel template which identifies which bacterial strain is in each well.(Use a unique code name such as TR-1 --Tues.lab Red group- strain 1.) Make a copy of the template in your lab notebook.
4. Your instructor will add the ladder marker and a positive control and start the current when all students have loaded their samples.
5. When the gel has finished (usually 45 min. at 100volts), your instructor will photograph it under UV light, label the lanes from the template, and post the photo to the data folder on the conference.

How will you judge a successful amplification? How many fragments and of what size do you expect to see? Remember that you used the same "universal" bacteria primer pairs that we used in our other amplification of 16s rDNA from the genomic soil DNA extract but you used a less "picky" DNA polymerase, Taq, rather than an expensive proof-reading polymerase.

We will clean up all the successful amplifications.

Culturable Bacteria Identification continued

Read last weeks tests, Continue with new tests Enterotube? Antibiotic sensitivity etc set up nitogen recycling tests add other "role" tests Other ideas?

Links to Labs

Lab 1
Lab 2
Lab 3
Lab 4
Lab 5
Lab 6
Lab 7
Lab 8
Lab 9
Lab 10
Lab 12