BME103:T930 Group 16

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Contents

Group 16

Name: Omar Moreno Salinas, and Rachel JuettenOpen PCR, ImageJ Software Processor, Data Compiler, and Analyzers
Name: Omar Moreno Salinas, and Rachel Juetten
Open PCR, ImageJ Software Processor, Data Compiler, and Analyzers
Name: Maggie McClure, and Swetha SwaminathanProtocol Persons: Sample Prep & Application
Name: Maggie McClure, and Swetha Swaminathan
Protocol Persons: Sample Prep & Application
Name: Marianna SinghDNA Measurement Operator
Name: Marianna Singh
DNA Measurement Operator
Name: Muawiya Ali Al-KhalidiR&D Scientist
Name: Muawiya Ali Al-Khalidi
R&D Scientist

LAB 1 WRITE-UP

Initial Machine Testing

The Original Design
Image:group 16.png


Experimenting With the Connections

When the heat sink is unplugged from the circuit board, the LCD screen is turned off. When we unplugged the white wire that connected the circuit board to the heating block the temperature reading on the LCD screen dropped drastically.

Test Run

We first tested open PCR on October 18, 2012. We learned how to take accurate temperatures using the open PCR machine. Using open PCR we were able to make a polymerase chain reaction. In order for this to occur, open PCR had to send the DNA through different sets of temperatures to heat it up to separate the strands and expose the bases, then cool it down for the primers to bind to the sequences, and also heat it back up to attain an extension of the copy of the new DNA. Which was conducted in an hour and thirty minutes.




Protocols

Polymerase Chain Reaction

Reagent Volume
Template DNA (20ng) 0.2 μL
10 μM forward primer 1.0 μL
10 μM reverse primer 1.0 μL
GoTaq master mix 50.0 μL
dH2O 47.8 μL
Total Volume 100.0 μL

Here is the patient information:


92136 M 54 Years


62276 F 61 Years

Flourimeter Measurements

Image:FlouimeterMeasurements.jpg




Research and Development

Specific Cancer Marker Detection - The Underlying Technology

A Polymerase chain reaction is a machine that amplifies a single or a few strands of DNA to generate millions of copies of that DNA sequence. Using this technology scientists can determine whether a patient has a positive or negative result towards cancer. A method of getting this data is called the PCR detection method, a method that relies on thermal cycling, switching back and forth to melt DNA and then connect primers. This is a method that can be used to detect whether a patient has positive result for cancer, because a sample of DNA can be taken and whether that connects to the primers and creates a chain reaction, scientists can then determine whether this DNA is positive or negative towards cancer. An example of proving this method can be seen using the r17879961 SNP, a cancer-associated sequence, using the PCR detection method we can prove that r17879961 SNP is actually associated with cancer. Because it carries with the Polymerase chain reaction, and to further prove the patient has a positive result for cancer, we use fluorescent dye and if the DNA glows in the solution, then the results are positive for cancer.

(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.)




==Results==

Sample Integrated Density DNA μg/mL Conclusion
PCR: Negative Control 9880697 F6 G6
PCR: Positive Control 4981557 F7 G7
PCR: Patient 1 ID #####, rep 1 14455570 F8 G8
PCR: Patient 1 ID #####, rep 2 8591662 F9 G9
PCR: Patient 1 ID #####, rep 3 13212871 F10 G10
PCR: Patient 2 ID #####, rep 1 12472923 F11 G11
PCR: Patient 2 ID #####, rep 2 22091168 F12 G12
PCR: Patient 2 ID #####, rep 3 11477553 F13 G13


KEY

  • Sample =
  • Integrated Density =
  • DNA μg/mL =
  • Conclusion =


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