BME103:T930 Group 12 l2: Difference between revisions

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'''Illustration'''<br>
'''Illustration'''<br>


[[Image:Shpoople.png‎|200px|illustration]]
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<!--- Include an illustration that shows how your system's primers allow specific amplification of the disease-related SNP --->
<!--- Include an illustration that shows how your system's primers allow specific amplification of the disease-related SNP --->



Revision as of 17:45, 28 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 TEAM

Name: Divya Amrelia
PCR engineer
Name: David Tze
PCR engineer
Name: Nathan Moore
Protocol Planner
Name: Philip Remick
Protocol Planner
Name: Ryan Magnuson
R&D Scientist

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 design manipulates the 4x4 PCR Tube Block to a 3x7 block capable of holding 21 DNA sample spaces instead of the generic 16. One of the 21 test tube spaces will be inserted with a platinum temperature sensor. The platinum temperature sensor reads the temperature more accurately, and since it reads the temperature more accurately it saves more time.


Key Features
PCR Tube Block In the new design, the PCR Tube Block has been expanded to 21 spaces to encompass more DNA samples.


Instructions





Protocols

Materials


PCR Protocol



DNA Measurement Protocol



Research and Development

Background on Disease Markers



Primer Design



Illustration

illustration