BME100 s2014:W Group14 L5: Difference between revisions

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'''Sample w/ DNA'''
'''Sample w/ DNA'''
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[[Image:BME100_Lab5_Group14_withDNA_sample.PNG|350px]]  [[Image:BME100_Lab5_Group14_withDNA_sample2.JPG|350px]]
[[Image:BME100_Lab5_Group14_withDNA_sample.PNG|350px]]  [[Image:BME100_Lab5_Group14_withDNA_sample2.JPG|300px]]
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'''Image J Values for All Samples'''  
'''Image J Values for All Samples'''  

Revision as of 21:18, 15 April 2014

BME 100 Spring 2014 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: Jose Duran
Name: Shawn Garcia
Name: Christian Keefer
Name: Karthik Puncha
Name: Austin Tielke

LAB 5 WRITE-UP

Background Information

SYBR Green Dye
[Instructions: A short summary describing SYBR green dye]


Single-Drop Fluorimeter
[Instructions: A description of the single-drop fluorimeter device. Add a PHOTO for bonus points]

How the Fluorescence Technique Works
[Instructions: In your own words]



Procedure

Smart Phone Camera Settings

  • Type of Smartphone: Apple iPhone 5S
    • Flash: Off
    • ISO setting: Auto
    • White Balance: Auto
    • Exposure: High
    • Saturation: High
    • Contrast: Low

Calibration

The camera was set up by placing the iPhone 5S in the holding compartment of the lab equipment. It was measured to be 6 centimeters away from the origin of the light emission. The settings (stated above) were adjusted; the height of the fluorimeter was adjusted in order to achieve a perfect side-angle perspective of the "beach ball" shaped liquid drop.

  • Distance between the smart phone cradle and drop = 8 centimeters


Solutions Used for Calibration

Initial Concentration of 2X Calf Thymus DNA solution (μg/mL) Volume of the 2X DNA solution (μL) Volume of the SYBR GREEN I Final DNA concentration in SYBR Green I solution (μg/mL)
5 80 80 2.5
2 80 80 1.0
1 80 80 0.5
0.5 80 80 0.25
0.25 80 80 0.125
0 80 80 0


Placing Samples onto the Fluorimeter

  1. Before placing samples onto the fluorimeter, turn on the Blue LED light & have the camera on the smartphone ready.
  2. Insert the glass sampling surface, with the smooth side facing down.
  3. Position the glass sampling surface so that the light emits between the first two rows of the glass.
  4. Place an 80 μL drop of SYBR Green I in the middle of the first two rows.
  5. Swap out the pipette tip with a new tip.
  6. Place an 80 μL drop of a specifically concentrated Calf Thymus DNA solution onto the top of the previously placed SYBR Green I drop. Every three 160 μL sample drops will vary in concentrated Calf Thymus DNA solution.
  7. In order to place a new sample drop, remove the 160 μL solution, move the glass sampling surface to the next two available rows, and repeat the process of placing two new 80 μL drops onto each other (as stated before).


Data Analysis

Representative Images of Samples

Sample w/o DNA




Sample w/ DNA



Image J Values for All Samples

[Instructions: See worksheet page 8. To save time on typing a new Wiki table from scratch, use THIS TOOL to auto-generate a Wiki table: Excel-to-Wiki Converter. Copy the headers and values from the Excel spreadsheet you made, paste them into the form field, click submit, copy the Wiki code that the tool generated, and replace TABLE GOES HERE (below) with your auto-generated code.]


TABLE GOES HERE


Fitting a Straight Line

[Instructions: Place an IMAGE of your Excel plot with a line of best fit here. See worksheet page 9]