To test the machine and it's connectivity several simple tests were run. First we unplugged the LCD display from the CPU, which caused the LCD display to lose power. We also unplugged the connection between the circuit board and the main heating block. After this connection was severed the LCD displayed a reading of -40 °C.
Test Run
October 25, 2012: We used machine number 11 to perform our PCR. The OpenPCR machines in the class showed lots of variation in overall run times, with our machine running on the slower side of the class average. We assume this reflected the individual machine's ability to transition between temperature cycles. The OpenPCR did finish the cycling and based on the second part of our experiment it successfully amplified our DNA sequence.
Protocols
Polymerase Chain Reaction
How it Works
In order to analyze genomes and genes,scientists have used polymerase chain reaction (PCR) techniques to amplify DNA. Multiple copies of DNA sequences much be made to be able to better view specific aspects of a gene due to the fact that isolated DNA samples are too small to view individually. In a test tube, PCR takes place by copying short fragments of DNA over and over again, also known as amplification. By altering the temperature within the test tubes, this allows the DNA strands to separate (boiling), bind to primers (cooled),and catalyze (warmed) to double the amount of DNA fragments after each cycle. By repeating each cycle the amount to DNA grows exponentially as two copies are made per strand.
How to Amplify a Patient's DNA Step 1-
After the Patients DNA is placed in to the test tubes along with the Master Mix, the tubes are placed into the PCR machine. Step 2-
As the machine warms to almost a boil, at 95 degrees Celsius, the DNA strands will begin to separate. Step 3-
Once the PCR machine has cooled down to 57 degrees Celsius, the primer will bind to the target sequence. Step 4-
The PCR machine needs to then warm back up to 72 degrees Celsius in order for extension of DNA to occur. This initiates the taq function where the taq protein, along with magnesium chloride, takes free floating nucleotides (DNTPs) and attaches them to the DNA stand in a reverse direction. Step 5-
Once steps 2-4 are repeated several times, each cycle will create newly replicated DNA stands and allow replication to continue until Master Mix is used up.
PCR Master Mix Components
For a 50µl reaction volume:
-GoTaq® Colorless Master Mix: 25µl
-Upstream primer: 10µM
-Downstream primer: 10µM
-DNA template 1–5µl
-Nuclease-Free Water to 50µl
Substances in Test Tubes
Reagent
Volume
Template DNA (20 ng)
.2 μL
10 μM forward primer
1.0 μL
10 μM reverse primer
1.0 μL
GoTaq master mix
50.0 μL
dH20
47.8 μL
Total Volume
100.0 μL
Patient Numbers
Patient #29341 is female at the age of 53.
Patient #23292 is male at the age of 56.
Flourimeter
Flourimeter Setup
Flourmeter Assembly Procedure Step 1-
Unclasp the black box and place it upside down to make a shade Step 2-
Place the assembly that is holding the slide inside the box Step 3-
Use the pipette to place a little over 2 drops of sample on the slide Step 4-
Turn on the blue light Step 5-
Position the slide so that the light goes directly through the drop Step 6-
Place a smartphone in the stand and position it so that the drop is in the picture
Saving Images to ImageJ Step 1-
Send the pictures from the phone to the email (make sure to keep track of which picture goes to which sample) Step 2-
Open our email on the computer and download the attached pictures on to the computer's picture file Step 3-
Open the ImageJ Step 4-
Click file and then click open (and the files from your computer open up) Step 5-
Click the desired picture and it will open up on ImageJ
Research and Development
Specific Cancer Marker Detection - The Underlying Technology
Polymerase Chain Reaction (PCR) works by adding primers, nucleotides, a catalyst, and a polymerase to a sample of DNA. Then the samples are placed in PCR machine which will cycle through the heats 95 degrees celsius to 57 degrees celsius to 72 degrees celsius and repeat that cycle thirty times. When the temperature is 95 degrees the DNA double helix denatures into individual single strands. After which, when the temperature is lowered to 57 degrees, the primers anneal to the single strand of DNA in preparation for replication. Then the sample is heated to 72 degrees Celsius where TAQ polymerase copies all the DNA after the primers. Given everything else for the PCR reaction the success of reaction depends on whether or not the primers placed in the mixture match some segment on the DNA strand. In this case the primers match with the known r17879961 (CHEK2) cancer-related segment were placed into mixture with the DNA. Specifically the forward primer is: TGGTATAAGACATTCCTGTC and the reverse primer is: AACTCTTACACTGCATACAT. The specific change in these primers occurs with the change from the typical CHEK2 gene at the 8,511,656 base pair (the 11th nucleotide in the reverse primer) where a cytosine is replaced by a thymine. Therefore only DNA segments that match these primers will be amplified. This method of replicating DNA works by having the two primers anneal to different strands of DNA and replicating in one direction. This process leaves two partial strands of DNA which is not the target sequence, however, it does contain the target sequence. Over the next few cycles the other primer will anneal to the same strand of DNA (if the forward annealed to it first then the reverse will anneal to it and vice versa). After annealing it will copy in the other direction and end where the other primer started giving you the 200 base pair target sequence. Because only segments with the primers are amplified if the patient does not have this r17879961 single nucleotide polymorphism (SNP) the DNA will not be amplified. Therefore the positive result for having the r17879961 SNP is the presence of amplified DNA in the PCR reaction.
Pray, Leslie A., Ph.D. "The Biotechnology Revolution: PCR and the Use of Reverse Transcriptase to Clone Expressed Genes." Nature.com. Nature Publishing Group, 2008. Web. 15 Nov. 2012.
Results
Procedure using Droid Phone
Image Number
Drop 1
Drop 2
Comments
210
SYBRGreen
-Control
*
211
SYBRGreen
2-1
*
212
SYBRGreen
2-2
*
213
SYBRGreen
2-3
*
214
SYBRGreen
+Control
Very Green
215
SYBRGreen
1-1
*
216
SYBRGreen
1-2
*
217
SYBRGreen
1-3
*
218
SYBRGreen
Red
Very Green
Sample
Area
Mean Pixel Value INTDEN
RAWINTDEN
INTDEN
Patient 1-Sample 1
21392
108.197
2314551
2314551
Patient 1-Sample 2
32248
111.873
3607696
3607696
Patient 1-Sample 3
35600
101.153
3601038
3601038
Negative Control
22928
150.115
3441833
3441833
Positive Control
38596
219.663
8478127
8478127
Patient 2-Sample 1
19316
104.921
2026652
2026652
Patient 2-Sample 2
29968
133.532
4001694
4001694
Patient 2-Sample 3
29556
*
*
*
Red
*
*
*
*
Description
Eppendorf Tube Label
Pipette Label
*
*
*
Description
INTDEN with background subtracted
DNA Concentration (μg/mL)
*
*
*
Sample
Integrated Density
DNA μg/mL
Conclusion
PCR: Negative Control
3367501
0
G6
PCR: Positive Control
8381066
1.193299682
G7
PCR: Patient 1 ID #####, rep 1
2222463
-0.266289229
G8
PCR: Patient 1 ID #####, rep 2
3515595
0.040183055
G9
PCR: Patient 1 ID #####, rep 3
3523638
0.042089246
G10
PCR: Patient 2 ID #####, rep 1
1944235
-0.3322296265
G11
PCR: Patient 2 ID #####, rep 2
3891599
0.129296003
G12
PCR: Patient 2 ID #####, rep 3
4210772
0.204940004
G13
KEY
Sample = is the specfic amount of DNA from the population, which is a cancer patient.
Integrated Density = is the total of the gray values of each pixel in a determined area.
DNA μg/mL = was found by using the negative and positive controls to create a curve in which each of the integrated density values could be substituted for the x value in the curve equation.
Conclusion = tells us if the patient is positive or negative for the cancer gene.
BME 103 Fall 2012
