BME100 f2013:W900 Group14 L4: Difference between revisions

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Wednesday, October 23, 2013<br>
Wednesday, October 23, 2013<br>
During our test run, we had some difficulty starting up the machine, as it had troubles starting up the process, and was constantly changing the time needed to create the first batch.





Revision as of 23:52, 29 October 2013

BME 100 Fall 2013 Home
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Lab Write-Up 1 | Lab Write-Up 2 | Lab Write-Up 3
Lab Write-Up 4 | Lab Write-Up 5 | Lab Write-Up 6
Course Logistics For Instructors
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Wiki Editing Help


OUR TEAM

Name: Rachael Brard
Role(s)
Name: Andrew Cable
Role(s)
Name: Austin Davis
Role(s)
Name: Omar Eltohamy
Role(s)

LAB 1 WRITE-UP

Initial Machine Testing

The Original Design
http://openwetware.org/images/thumb/e/ef/HALEY.png/562px-HALEY.png
http://www.wired.com/reviews/wp-content/uploads/2011/12/reviews_pcr_f.jpg
PCR stands for polymerase chain reaction. The PCR machine depicted here is a biochemical technology that when used properly can amplify a selected piece of dna to make millions of copies. This machine heats dna to break it apart, then cools it so that the polymerase will attach to the dna strands and make copies.

Experimenting With the Connections

When we unplugged (part 3) from (part 6), the machine's screen went black. The LCD screen did not receive power while the rest of the machine still did.

When we unplugged the white wire that connects (part 6) to (part 2), the machine did not read temperature properly. It briefly fluctuating upon detaching the wire, then read -40 degrees C.


Test Run

Wednesday, October 23, 2013
During our test run, we had some difficulty starting up the machine, as it had troubles starting up the process, and was constantly changing the time needed to create the first batch.




Protocols

Thermal Cycler Program


DNA Sample Set-up

row 1 cell 1 row 1 cell 2 row 1 cell 3 row 1 cell 4
row 2 cell 1 row 2 cell 2 row 2 cell 3 row 2 cell 4


DNA Sample Set-up Procedure

  1. First, the sample of DNA to be amplified is added.
  2. Both DNA primers are then added in succession.
  3. DNA Taq Polymerase is then added to the vials.
  4. Finally, loose nucleic acids are added so as to form the DNA copies

PCR Reaction Mix

  • The PCR reaction mix is a combination of DNA to be amplified, two DNA primers, which allow for DNA Taq Polymerase to read and copy the desired sequence, DNA Taq Polymerase, for copying and reading the desired DNA, and nucleic acids, which are used to form the new copies of DNA.

DNA/ primer mix

  • What is in the DNA/ primer mix?





Research and Development

PCR - The Underlying Technology

(Add a write-up, essay-style, organized into paragrpahs with descriptive headers, based on the Q&A's from Section three of your worksheet)

(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 PCR video/ tutorial might be useful. Be sure to credit the sources if you borrow images.)