BME103:T930 Group 10 l2: Difference between revisions
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2. Use properly labeled micropipette to place 17 samples into 17 properly labeled Eppendorf tubes already containing 50 microliters GoTaq mix. To see contents of GoTaq mix, see materials.<br> | 2. Use properly labeled micropipette to place 17 samples into 17 properly labeled Eppendorf tubes already containing 50 microliters GoTaq mix. To see contents of GoTaq mix, see materials.<br> | ||
3. Place 17 Eppendorf tubes in Open PCR. This PCR machine is made of steel in order to decrease safety hazards, and is able to hold more Eppendorf tubes. Therefore, all 17 Eppendorf tubes fit in this PCR. The top of the PCR machine | 3. Place 17 Eppendorf tubes in Open PCR. This PCR machine is made of steel in order to decrease safety hazards, and is able to hold more Eppendorf tubes. Therefore, all 17 Eppendorf tubes fit in this PCR. The top of the PCR machine snaps shut and can be clipped down to be less dangerous. <br> | ||
4. To make up for the more Eppendorf tubes in the PCR machine, each cycle is increased by 2 degrees Celsius, making the Thermal Cycler program: <br> | 4. To make up for the more Eppendorf tubes in the PCR machine, each cycle is increased by 2 degrees Celsius, making the Thermal Cycler program: <br> | ||
Stage One: 1 cycle, 97 degrees Celsius for 180 seconds<br> | Stage One: 1 cycle, 97 degrees Celsius for 180 seconds<br> |
Revision as of 11:07, 15 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 2 WRITE-UPThermal Cycler EngineeringOur re-design is based upon the Open PCR system originally designed by Josh Perfetto and Tito Jankowski.
Key Features
Instructions
ProtocolsMaterials
For PCR Protocol
1. PCR machine
1. Label Eppendorf Tubes with 1-17, 2 for positive and negative controls and the rest for the patients DNA. Each tube should contain 50 microliters of one of the following substances:
2. Use properly labeled micropipette to place 17 samples into 17 properly labeled Eppendorf tubes already containing 50 microliters GoTaq mix. To see contents of GoTaq mix, see materials. DNA Measurement Protocol 1. With permanent marker, clearly number micropipettes. With permanent marker, number Eppendorf tubes at the top. There should be 17 labeled micropipettes and 17 Eppendorf tubes. Research and DevelopmentBackground on Disease Markers
Primer Design
Illustration
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