BME103:T930 Group 6 l2: Difference between revisions

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'''PCR Protocol'''
'''PCR Protocol'''


1. Using a micro-pipette, transfer 1.0-1.5 mL of desired DNA sample into at least three test tubes.
2. reagent solution
3. place tubes into holder in PCR machine
4. program cycles on OpenPCR
5. Run reaction





Revision as of 11:48, 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 TEAM

Name: Nicholas Sterkowitz
Open PCR machine engineer
Name: Dominic Ilardi
Open PCR machine engineer
Name: Alexandra Nazareno
Experimental Protocol Planner
Name: Amanda Sweig
Experimental Protocol Planner
Name: Taylor Deegan
Research and Development(s)

LAB 2 WRITE-UP

Thermal Cycler Engineering

Our re-design is based upon the Open PCR system originally designed by Josh Perfetto and Tito Jankowski.


System Design


Key Features


Instructions





Protocols

Materials

Supplied in PCR Kit Amount
PCR Machine 1
Fluorometer Box 1
Calf Thymus 0.5 mL
SYBR Green (diluted) 1.5 mL
Camera Stand 1
Glass Plates 2
Calibration DNA 0.5 mL
GoTaq Polymerase and Buffer Solution 10 mL
Small Test Tubes 25
Large Test Tubes 25


Supplied by User Amount
Smartphone Camera 1
Laptop 1
ImageJ Download 1
Power Supply 1
DNA Sample At least 3 samples


PCR Protocol

1. Using a micro-pipette, transfer 1.0-1.5 mL of desired DNA sample into at least three test tubes.

2. reagent solution

3. place tubes into holder in PCR machine

4. program cycles on OpenPCR

5. Run reaction


DNA Measurement Protocol

Research and Development

Background on Disease Markers



Primer Design



Illustration