BME103:T930 Group 14: Difference between revisions

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==Results==
==Results==


(Your group will add the results of your Fluorimeter measurements from Week 4 here)
 
<!--- Place two small Image J data images here. One showing the result of Water and the other showing the result of Calf Thymus DNA --->
 
 
<!--- Enter the values from your group's Data Analyzer table below. E6, F6, etc. are the excel cells from which you should copy your data. --->
{| {{table}}
|- style="background:#f0f0f0;"
| '''Sample''' || '''Integrated Density''' || '''DNA μg/mL''' || '''Conclusion'''
|-
| PCR: Negative Control || E6 || F6 || G6
|-
| PCR: Positive Control || E7 || F7 || G7
|-
| PCR: Patient 1 ID #####, rep 1 || E8 || F8 || G8
|-
| PCR: Patient 1 ID #####, rep 2 || E9 || F9 || G9
|-
| PCR: Patient 1 ID #####, rep 3 || E10 || F10 || G10
|-
| PCR: Patient 2 ID #####, rep 1 || E11 || F11 || G11
|-
| PCR: Patient 2 ID #####, rep 2 || E12 || F12 || G12
|-
| PCR: Patient 2 ID #####, rep 3 || E13 || F13 || G13
|}
 
 
KEY
* '''Sample''' = <!--- explain what "sample" means --->
* '''Integrated Density''' = <!--- explain what "integrated density" means and how you did background subtraction to get this value --->
* '''DNA μg/mL''' = <!--- explain how you calculated this --->
* '''Conclusion''' = <!--- explain what "Positive" and "No signal" means, relative to the control samples --->





Revision as of 14:23, 9 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: Jake Lindquist
Protocol Planner
Name: Breanna Pratt
Protocol Planner
Name: Kirsten Jefferys
Open PCR Machine Engineer
Name: Carlos Duarte
Research and Design Scientist
Name: Ben Alcron
Open PCR Machine Engineer
Name: Bryce DeSimmone
Research and Design Scientist

LAB 1 WRITE-UP

(Please finish by 11/14/2012)

Initial Machine Testing

The Original Design




Description of Open PCR Device


Experimenting With the Connections

When we unplugged the LED from the Open PCR circuit board, the machine stop displaying information on the LED screen.

When we unplugged the white wire that connects the Open PCR circuit board to main heat sink, the machine incorrectly displays the temperature as negative 40 degrees Celsius.

Test Run

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




Protocols

Polymerase Chain Reaction

Reagent Volume
Template DNA (20 ng) .2 μL
10 μM forward primer 1.0 μL
10 μM reverse primer 1.0 μL
GoTaq master mix 50.0 μL
dH2O 47.8 μL
Total Volume 100.0 μL


Fluorimeter Measurements

(Add your work from Week 3, Part 2 here)




Research and Development

Specific 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.)




Results

Sample Integrated Density DNA μg/mL Conclusion
PCR: Negative Control E6 F6 G6
PCR: Positive Control E7 F7 G7
PCR: Patient 1 ID #####, rep 1 E8 F8 G8
PCR: Patient 1 ID #####, rep 2 E9 F9 G9
PCR: Patient 1 ID #####, rep 3 E10 F10 G10
PCR: Patient 2 ID #####, rep 1 E11 F11 G11
PCR: Patient 2 ID #####, rep 2 E12 F12 G12
PCR: Patient 2 ID #####, rep 3 E13 F13 G13


KEY

  • Sample =
  • Integrated Density =
  • DNA μg/mL =
  • Conclusion =