BME103:T130 Group 14 l2

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(OUR TEAM)
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| [[Image:Ganondorf.png|100px|thumb|Name: Nathaniel Bennett<br>Role: Software Designer]]
| [[Image:Ganondorf.png|100px|thumb|Name: Nathaniel Bennett<br>Role: Software Designer]]
| [[Image:Sheikh.jpg|100px|thumb|Name: Hanna Rahman<br>Role: Protocol Design ]]
| [[Image:Sheikh.jpg|100px|thumb|Name: Hanna Rahman<br>Role: Protocol Design ]]
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| [[Image:BME103student.jpg|100px|thumb|Name: Hope Haddad<br>Role: Research and Development Specialist]]
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| [[Image:Princess_Zelda.png|100px|thumb|Name: Hope Haddad<br>Role: Research and Development Specialist]]
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Revision as of 16:29, 29 November 2012

BME 103 Fall 2012 Home
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Lab Write-Up 1
Lab Write-Up 2
Lab Write-Up 3
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Contents

OUR TEAM

Name: Brian HeddenRole: Software Designer
Name: Brian Hedden
Role: Software Designer
Name: Nathaniel BennettRole: Software Designer
Name: Nathaniel Bennett
Role: Software Designer
Name: Hanna RahmanRole: Protocol Design
Name: Hanna Rahman
Role: Protocol Design
Name: Hope HaddadRole: Research and Development Specialist
Name: Hope Haddad
Role: Research and Development Specialist

LAB 2 WRITE-UP

Thermal Cycler Engineering

Our re-design is based upon the Open PCR system originally designed by Josh Perfetto and Tito Jankowski.


System Design
Our redesign consisted of improving the insulation in the OpenPCR machine between the processing unit and fan and the the heating cap. This change is especially useful, allowing for increased insulation, with material such as fiberglass. This increased insulation allows for a more constant temperature at the heating cap. Because the temperature at the heating cap will be more constant, the OpenPCR machine will be able to perform its job faster and more efficiently, which is an incredibly handy feature considering a normal PCR machine can take up to two hours to amplify DNA. However, this increased insulation will cause the machine to become increasingly hot as it does its job. Our redesign accounts for this problem. By improving the fan on the machine as well, we eliminate any potential problems due to heat, such as overheating. However, another problem that arises from these new additions to the machine is room. The machine itself is fairly small, and compromising this portable size is not an option. For that reason, the redesign includes the use of a smaller fan, maintaining the intended efficiency of the redesign while accounting for the possible compromise in size. This redesign helps to improve the time that it takes for the OpenPCR machine to amplify DNA while maintaining a similar, if not smaller, size, allowing for much more DNA to be amplified in the same amount of time.

Key Features

-Improved fiberglass insulation
-Efficient smaller fan
-Faster DNA amplification

Instructions


The Open PCR machine is fairly easy to use. Simply plug it in to the USB port on your computer and turn it on. From your computer, you can adjust the temperature, add or remove steps to the process, and adjust the number of cycles. Even though the inside of the machine was redesigned, the instructions on how to use the machine have not changed.





Protocols

Materials

Supplied in the Kit Amount
PCR Machine 1: $400- $600
Fluorimeter (LED glass stand) 1: $ 200.00
Connection USB cord for Computer to PCR 1 1: $20.00
Smartphone Stand 1: $ 5.00
Box 1: $ 5.00
Disk for ImageJ 1: $ 0.50
Improved Insulation 1: ~ $ 200.00
Efficient Smaller Fan 1: $ 50.00



Supplied by User Amount
Computer 1: $ 1000
Pipettes 16 : $ 0.25 (16X)
Glass Slides 2 : $1.00 (2X)
Smartphone 1: $ 150.00
Small Tubes 32: $ 4.00
Water Varies
DNA Samples Varies



Reagent Volume
Template DNA ( 20 nanograms) 0.2 microliters
10 micrometers forward primer 1.0 microliters
10 micrometers reverse primer 1.0 microliters
GoTaq Master Mix 50.0 microliters
Distilled Water 47.8 microliters
Total Volume 100.0 microliters



PCR Protocol

Setting up your Tubes

  1. Collect 8 samples of DNA and 1 DNA(calf thymus standard at 2 micrograms/mL) sample and water from the scintillation vial to analyze.
  2. With a permanent marker, number the transfer pipettes at the bulb so that you limit cross-contamination and only use ONE per solution, and number your Eppendrof tubes at the top. At the end, you should have 10 Eppendorf tubes and 10 pipettes clearly labeled.
  3. Transfer each sample separately ( using one pipette per sample) into an Eppendorf tube containing 400 mL of buffer. Label this tube with the number of your sample. Make sure to transfer all of the sample into the Eppendorf tube. Use the same pipette to place ONLY this sample's drop onto the fluorescent measuring device.
  4. Take the specially labeled Eppendorf tube containing the SYBR GREEN I and using it's assigned pipette, place two drops on the first two centered drops.
  5. Now take the diluted sample and place two drops on top of the SYBR GREEN I solution drops.
  6. Align the light going through the drop.
  7. Take pictures with the smartphone, as many as desired.
  8. If you are not satisfied with that sample, you may rerun that sample again or move on to the next sample.
  9. Be sure to only run 5 samples per slide.
  10. Before completing the lab, run the water from the scintillation vial as a BLANK using the same procedure listed above.



Smartphone Settings

  1. Turn off the flash
  2. Set ISO to 800
  3. Set white balance to auto
  4. Set exposure to the highest setting
  5. Set saturation to the highest setting
  6. Set contrast to lowest setting



PCR Machine

  1. Acquire the DNA samples that have been submitted for testing
  2. Insert Reactants into respective PCR tubes
  3. Connect the PCR machine to the computer and press 'Start' to record data
  4. Run the DNA samples through the thermal cycler program (see Stage 1)
    1. Stage 1 (Initiation): 1 cycle at 95°C for 3 minutes, to separate the DNA strand.
    2. Stage 2 (Denaturation): 35 cycles: first at 95°C for 30 seconds, and then gradually decrease the temperature to approximately 57°C for 30 seconds, and then raise the temperature to approximately 72°C for 30 seconds, so the DNA polymerase can be activated. This is also an example of heat shock, and is effective to initiate the addition of complementary nucleotides onto the DNA strand, which the DNA polymerase does.
    3. Stage 3 (Elongation) : At this step, hold the DNA at 72°C for 3 minutes.The temperature is held here so that the DNA polymerase can copy the strand. Also, this is where the two desired fragments begin to appear- two strands that begin with primer one and end with primer two- and these are the DNA copies of the segment of DNA you began with.
    4. Stage 4: Final hold until the DNA stabilizes at 4°C. At the end of this cycle you will have 8 fragments of the DNA
  5. After the DNA has been through the numerous cycles, you will have over thousands of fragments of the same DNA sequences. After the DNA has been through the thermal cycle, mix each DNA sample with the PCR reaction mix (Taq DNA polymerase, MgCl2, dNTP’s, and a forward and reverse primer), using a separate pipette each time to reduce cross-contamination into 8 separate tubes



Image Processing

  1. Upload pictures to ImageJ
  2. Click on 'Analyze', choose 'Set Measurements', then 'Area Integrate Density', and 'Mean Gray Value'
  3. Click 'Image', choose 'Color', and then 'Split Channels' to create three files
  4. Choose image name that has 'green'
  5. Select the 'Oval Selection' on the Menu Bar.
  6. Click and stretch oval around green or clear drop in image. Click 'Analyze' and choose 'Measure'
  7. Record sample number and measurements
  8. Draw another oval of the same size in the 'green' file for the background above the drop to get the 'noise.' Click 'analyze' and choose 'measure'
  9. Record sample name and measurements and use as background label
  10. Save measurements to Excel file.

DNA Measurement Protocol

Research and Development

Background on Disease Markers



Primer Design



Illustration


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