BME103:T130 Group 9: Difference between revisions
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==Results== | ==Results== | ||
'''DNA Concentration and Analysis''' | |||
{|border="1" class="wikitable" style="text-align:center; width:300px; height:300px;" | |||
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|'''Description''' | |||
|'''INTDEN with background subtracted''' | |||
|'''DNA Concentration μg/mL''' | |||
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!Water Blank | |||
|8958||0 | |||
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!DNA Calf Thymus | |||
|94731||2 | |||
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!Positive Control | |||
|91845||1.939 | |||
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!Negative Control | |||
|20445||0.432 | |||
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!46 Yr Female 1 | |||
|24592||0.519 | |||
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!46 Yr Female 2 | |||
|15887||0.335 | |||
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!46 Yr Female 3 | |||
|11427||0.241 | |||
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!62 Yr Male 1 | |||
|82018||1.733 | |||
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!62 Yr Male 2 | |||
|73441||1.551 | |||
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!62 Yr Male 3 | |||
|78932||1.66 | |||
|} | |||
[[Image: Results.png]] | [[Image: Results.png]] | ||
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Revision as of 15:28, 8 November 2012
BME 103 Fall 2012 | Home People Lab Write-Up 1 Lab Write-Up 2 Lab Write-Up 3 Course Logistics For Instructors Photos Wiki Editing Help | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
OUR TEAMLAB 1 WRITE-UPInitial Machine Testing
When we unplugged the LCD from the Circut Board, the display was disconnected and would not appear.The PCR would still work. When we unplugged the white wire that connects the PCB Circut Board to Temperature Sensor, the machine would not be able to sense temperature correctly and would not give us a reading. Test Run (Write the date you first tested Open PCR and your experience(s) with the machine)
ProtocolsPolymerase Chain Reaction
Eight samples were tested during this investigation. These included: a positive control with the cancer DNA template, a negative control without the cancer DNA template, and three samples each from the two subjects. The first subject was a 46 year old woman, correlating to test tubes labeled 2, and the other was a 62 year old man, correlating to test tubes labeled 4. Fluorimeter Setup and Measurements
The next step is to analyze the resulting pictures by measuring the amount of pixels created by the light and comparing it to the controls. In order to measure this, the pictures must be analyzed using ImageJ software: Research and DevelopmentSpecific Cancer Marker Detection - The Underlying Technology Polymerase Chain Reaction (PCR) is a process by which we replicate DNA in order to determine specific sequences of DNA. In our specific lab, we used PCR to look for a sequence of nucleotides that signify cancer. On the surface level, we start with 2 strands of DNA, Magnesium Chloride (MgCl2), a TAQ enzyme, and DNTP, which is a mixture of the four bases – A, C, T, and G. We then set the PCR test to change temperatures after set periods of time to allow specific processes to work on the molecular level. We also add a fluorescent die that will bind to only the double strand of DNA. At the molecular level, the process begins by breaking the hydrogen bonds to separate the two DNA strands. This can only be done by heating the PCR tubes holding the DNA solution to 95°C. When the OpenPCR converts to 57°C, the reagent, called a “primer,” detects a specific sequence – in this case, a cancer-specific sequence. We construct this primer to bind to the forward string of DNA that is the partner sequence to the cancerous sequence. If the cancerous sequence is not present, then the primer only connects to the forward strand of DNA. If the cancerous sequence is present, then the primer connects to both. The temperature then changes to 72°C and the TAQ polymerase enzyme then replicates only the DNA strand(s) that the primer binds to. MgCl2 binds to the TAQ to help it function properly; the concentration of MgCl2 is directly related to the speed at which the TAQ restrings the DNA. This entire process occurs many many times in order to replicate the DNA over and over again (we usually set the openPCR experiment for 30 cycles). If the DNA is positive for cancer, the graph at the end of the experiment will be exponential because when it splits the two strings of DNA, the primer will find cancer on both strings of nucleotides. Both strings are then replicated, ergo the growth will be exponential. If the DNA is negative for cancer, the reagent will only attach to one of the strands and the graph will be more linear. Because the fluorescent die that we added in the beginning will only bind to the double strand of DNA, the DNA will glow (showing that there is an excessive amount of double stranded DNA- and thus cancer is present). If the DNA does not glow, there is no cancer present in the DNA.
ResultsDNA Concentration and Analysis
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