BME103 s2013:T900 Group4
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Lab Write-Up 1
Lab Write-Up 2
Lab Write-Up 3
Course Logistics For Instructors
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LAB 1 WRITE-UP
Initial Machine Testing
The Original Design
When we unplugged (part 3) from (part 6), the machine ... (did what? fill in your answer)
When we unplugged the white wire that connects (part 6) to (part 2), the machine ... (did what? fill in your answer)
(Write the date you first tested Open PCR and your experience(s) with the machine)
Thermal Cycler Program
DNA Sample, 50 μL each: patient ID's from the UnderGrad Teaching Assistant(UGTA).
DNA Sample Set-up Procedure
DNA/ primer mix
Research and Development
Specific Cancer Marker Detection - The Underlying Technology
First the DNA/Primer mix is combined with the PCR reaction mix in a small test tube. Repeat samples are advised to make sure that the results are consistent.
When the test tube is placed in a PCR machine, the mixture is heated to 95 degrees Celsius for 30 seconds. This high heat breaks apart complementary strands of DNA, exposing the nucleotides. The DNA strands are essentially cut in half lengthwise into two new strands.
The machine then rapidly cools to 57 degrees Celsius for 30 seconds, allowing the DNA primers to bind to the exposed sites. The DNA primers can only bind to the specific site they are complementary to, which allows researchers to target specific DNA sequences. Even if only one nucleotide is different, the primer does not bind well enough to stay. This means that researchers can choose a specific gene, such as one predisposing for cancer, and order a primer that binds only to that gene. If the specified gene is not present, the primer will not bind and the DNA will not be amplified.
Two different primers are needed: a forward primer and reverse primer. The forward primer binds to one "half" of the DNA sample, and the reverse primer binds to the other "half." If you picture the DNA as a train track, with each rail as one half of the DNA, one primer binds to one rail, and the other binds to the other rail at the opposite end of the track.
The mixture is then heated up to 72 degrees Celsius for 30 seconds. At this temperature, DNA polymerase binds to the primers and builds a new segment of complementary DNA with the free nucleotides in the mixture. Returning to the train track analogy, one rail is being built from right to left and the other from left to right, both being built towards each other. This is because DNA is read in one direction on one side, and a different direction (relative to the first) on the other.
So, if there was only one strand of DNA in the mixture originally, now there are two (since both halves have been replicated). The mixture is then reheated to 95 degrees and the cycle continues, each time doubling the amount of DNA in the mixture. This process usually continues for an hour or so, until there are billions of copies of DNA. This whole process is referred to as DNA amplification.
(BONUS points: Use a program like Powerpoint, Word, Illustrator, Microsoft Paint, etc. to illustrate how primers bind to the cancer DNA template, and how Taq polymerases amplify the DNA. Screen-captures from the OpenPCR tutorial might be useful. Be sure to credit the source if you borrow images.)