BME100 f2013:W1200 Group18 L4: Difference between revisions

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| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Carlyn Harris<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Tori Platt<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Nikhil Patel<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Alexandra Olson<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: Matthew Armas<br>Role(s)]]
| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
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Revision as of 19:18, 27 October 2013

BME 100 Fall 2013 Home
People
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
Photos
Wiki Editing Help


OUR TEAM

Name: Carlyn Harris
Role(s)
Name: Tori Platt
Role(s)
Name: Nikhil Patel
Role(s)
Name: Alexandra Olson
Role(s)
Name: Matthew Armas
Role(s)
Name: student
Role(s)

LAB 1 WRITE-UP

Initial Machine Testing

The Original Design
(Add image of the full OpenPCR machine here, from the Week 9 exercise. Write a paragraph description for visitors who have no idea what this is)


Experimenting With the Connections

When we unplugged (part 3) from (part 6), the machine ... (did what? fill in your answer)

When we unplugged the white wire that connects (part 6) to (part 2), the machine ... (did what? fill in your answer)


Test Run

(Write the date you first tested Open PCR and your experience(s) with the machine)




Protocols

Thermal Cycler Program
Heated Lid: 100°C
Initial Step: 95°C for 3 minutes
Next Step: 35 cycles, denature at 95°C for 30 seconds, anneal at 57°C for 30 seconds, extend at 72°C for 30 seconds
Final Step: 72°C for 3 minutes
Final hold: 4°C


DNA Sample Set-up
PCC= Positive control: Cancer DNA
NCC= Negative control: Non-cancer DNA
P11,P12,P13= Patient 1's DNA samples
P21,P22,P23= Patient 2's DNA samples
Patient 1 ID: 54174
Patient 2 ID: 43184


PCC P11 P12 P13
NCC P21 P22 P23


DNA Sample Set-up Procedure
1. Label 6 50 μL disposable pipette tips with the labels given below corresponding to each patient.
2. Label the remaining 2 50 μL pipette tips, one as the positive control cancer DNA (PCC) and one as the negative control non-cancer DNA (NCC).
3. Pipette the PCR reaction mix into each reaction tube.
4. Using a different disposable pipette tip for each sample, pipette the DNA sample primer mix into each reaction tube.
5. Place the reaction tubes in the thermal cycler.
6. Run the PCR software that follows the protocol below.


PCR Reaction Mix

The PCR reaction mix contains:

   -Tag DNA Polymerase
   -MgCl2
   -dNTP's


DNA/ primer mix

The DNA primer mix contains:

   -Different template DNAs
   -Forward primer
   -Reverse primer





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.)