BME103: Difference between revisions

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Image:BME103_Group9_FluorimeterSetup.jpg|A camera phone is placed in front of the fluorimeter.<br>Photo credit: [http://openwetware.org/wiki/BME103:W930_Group7 Thurs 9:30am Group 9]
Image:BME103_Group9_FluorimeterSetup.jpg|A camera phone is placed in front of the fluorimeter. Photo: [http://openwetware.org/wiki/BME103:W930_Group7 Thurs 9:30am Group 9]
Image:2012-11-01_11.53.50.jpg|A sample droplet is placed on a hydrophobic slide.<br>Photo credit: [http://openwetware.org/wiki/BME103:T930_Group_17 Thurs. 9:30am Group 17]
Image:2012-11-01_11.53.50.jpg|A sample droplet is placed on a hydrophobic slide. Photo: [http://openwetware.org/wiki/BME103:T930_Group_17 Thurs. 9:30am Group 17]
Image:Bme_103_group7_setup_diagram2.png|Digital rendition of the fluorimeter set-up.<br>Photo credit: [http://openwetware.org/wiki/BME103:W930_Group7 Wed 9:30am Group 7]
Image:Bme_103_group7_setup_diagram2.png|Digital drawing of the fluorimeter set-up. Image: [http://openwetware.org/wiki/BME103:W930_Group7 Wed 9:30am Group 7]
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Revision as of 01:50, 18 December 2012

BME 103 Fall 2012 Home
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Lab Write-Up 1
Lab Write-Up 2
Lab Write-Up 3
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Introduction to Biomedical Engineering - Lab Part 2

Learning Objectives: Students should leave this unit equipped with a theoretical understanding of how to detect DNA biomarkers and the relevance of this technology to human healthcare. Emphasis will be on good lab/experimental controls and the collection of statistically valid measurements. Students will also understand how commonly used lab devices function, and explore the recent efforts to simplify experiments and to lower costs. At the end of the section, students will explore creative new biosensor designs based on PCR and fluorescent imaging.


GETTING STARTED

  1. Create an OpenWetWare account: Fill in the form at OpenWetWare:How to join
  2. Edit your group's wiki: Find your group's Wiki template in one of the Lab Write-Up sections. There are further instructions there. Be creative and have fun editing!


THE COURSE IN REVIEW

Set-up: OpenPCR Building

Before this unit began, a group of ~10 upper level undergrads and graduate students assembled the OpenPCR machines. This was a great experience for the graduate students, and saved our Freshmen engineers the time and trouble of assembling the delicate pieces from scratch in a very limited amount of time. Thanks to our assembly team and Dr. Pizziconi's Design Studio team for your help!


Week 1: Introduction - DNA as a Biomarker, 10/17/12

Students were introduced to basic DNA science and its relationship to diagnostics and health. Sequence-specific DNA hybridization uses primers designed to base-pair with a target disease-associated marker. This leads to exponential amplification of an invisible DNA target. A mismatch (non-disease DNA sequence) does not produce amplification. Team members chose roles as Open PCR machine tester, Experimental protocol planner, and Research and development scientist.

Snapshot of the worksheet for planning PCR reactions.

In concurrent work sessions...

  • Open PCR machine testers partially disassembled, reassembled, and tested the OpenPCR thermal cycler with the guidance of a worksheet and the OpenPCR machine manual.
  • Experimental protocol planners planned a Polymerase Chain Reaction (PCR) protocol for the Open PCR system and programmed the machine for thermal cycling with the guidance of a worksheet.
  • Research and development scientists learned how the Polymerase Chain Reaction works so that they could explain the process to their teammates. This was done with the guidance of the instructor and the OpenPCR Virtual Lab tutorial.



Week 2: DNA Amplification Reactions, 10/24/12

Students used their experience from the previous week to set up and run a PCR experiment. The students were provided with personal protective equipment, 8 tubes of 50 μL PCR reaction mix, 8 tubes of 50 μL diluted template + primers. The instructors provided positive and negative "patient" samples so that some samples would test positive for a DNA marker (produce amplification), and others would test negative.

Activities:

  • Experimental protocol planners set up and ran the PCR reactions. These were set aside to run for ~2 hours.
  • Each team practiced operating the Single Drop Fluorimeter with plain water samples.

Students were introduced to a Single Drop Fluorimeter fluorescence-based DNA detection device that was designed by Dr. Garcia. When a natural or PCR-amplified double-stranded DNA sample is stained with SYBR green and exposed to a blue LED light, the drop fluoresces green. The signal is captured as an image with the user's camera phone.


Week 3: Computer-Aided Design with Solid Works, 10/31/12

Activities:

  • Open PCR machine engineers used Solid Works to explore the computer-aided design file of the Open PCR system (provided by Josh Perfetto, Open PCR).
  • Experimental protocol planners
  • Research and development scientists


Week 4: Measuring DNA Using Fluorescence, 11/7/12


Lab Report 1: Each team created a Wiki page write-up of their learning experiences

Week 5: Designing a New System, 11/14/12

Activities:

  • Open PCR machine engineers used Solid Works to explore the computer-aided design file of the Open PCR system (provided by Josh Perfetto, Open PCR).
  • Experimental protocol planners
  • Research and development scientists


Lab Report 2: Each team created a Wiki page write-up of their machine designs and protocols.

Week 6 & 7: Advertisement Videos, 11/28/12 & 12/6/12

Activities:

  • Open PCR machine engineers used Solid Works to explore the computer-aided design file of the Open PCR system (provided by Josh Perfetto, Open PCR).
  • Experimental protocol planners
  • Research and development scientists


Lab Report 3: Each team created an advertisement video for their new system.