BME103:W930 Group10: Difference between revisions
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| [[Image:BME103student.jpg|100px|thumb|Name: Susan Sajadi<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Susan Sajadi<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Raymond<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Raymond Feliciano<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Britny<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Britny Sepulveda<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Rachel Lundeen<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Rachel Lundeen<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Liz Lopez<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Liz Lopez<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Larry Moss<br>Role(s)]] | | [[Image:BME103student.jpg|100px|thumb|Name: Larry Moss<br>Role(s)]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Collin Siguenza <br>Role(s)]] | |||
| [[Image:BME103student.jpg|100px|thumb|Name: Rotem Berger<br>Role(s)]] | |||
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Revision as of 11:36, 31 October 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-UP(Please finish by 11/7/2012) Initial Machine TestingThe Original DesignThis is the OpenPCR machine used to automate polymerase chain reactions. This reaction allows for the amplification of specific DNA which useful for detecting different markers such as those indiciating an increased risk for cancer, presence of HIV, etc. Experimenting With the Connections When we unplugged the LCD screen from the Open PCR circuit board, the machine's LCD screen did not turn on. When we unplugged the white wire that connects Open PCR circuit board to the heat sink, there appeared to be no effect, however it is likely that the heat sink would not function during a trial.
On Oct. 24th, 2012 we first used the Open PCR machine to run 25 cycles on eight samples which included two sets of three samples and a positive and negative control. The process was succesful, taking ~90 minutes for the reaction to complete. Initial testing of the device indicated the machine and software were synced in regards to the temperature during each cycle.
ProtocolsPolymerase Chain Reaction (Add your work from Week 3, Part 1 here)
(Add your work from Week 3, Part 2 here)
Research and DevelopmentSpecific Cancer Marker Detection - The Underlying Technology (Add a write-up of the information discussed in Week 3's class) (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.) For an animated walkthrough of the process, check out this PCR Virtual Lab from the team at the University of Utah's Genetic Science Learning Center Works Cited
"Microbial Chatter." - Thermus Aquaticus. N.p., n.d. Web. 31 Oct. 2012.
"Replication." Shmoop. N.p., n.d. Web. 31 Oct. 2012.
Results(Your group will add the results of your Fluorimeter measurements from Week 4 here)
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