BME103 s2013:T900 Group2 L2: Difference between revisions
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{| {{table}} width=700 | {| {{table}} width=700 | ||
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| DNA final concentration ()|| Ave. Mean|| Ave. IntDen | | DNA final concentration (ng/mL)|| Ave. Mean|| Ave. IntDen | ||
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| | | 2.5 || row 2 cell 2 || row 2 cell 3 | ||
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| row 3 cell 1 || row 3 cell 2 || row 3 cell 3 | | row 3 cell 1 || row 3 cell 2 || row 3 cell 3 | ||
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| row 2 cell 1 || row 2 cell 2 || row 2 cell 3 | | row 2 cell 1 || row 2 cell 2 || row 2 cell 3 | ||
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| 0 || row 2 cell 2 || row 2 cell 3 | |||
|} | |} | ||
''[Add more rows as needed]'' | ''[Add more rows as needed]'' |
Revision as of 22:29, 1 April 2013
BME 103 Spring 2013 | Home People Lab Write-Up 1 Lab Write-Up 2 Lab Write-Up 3 Course Logistics For Instructors Photos Wiki Editing Help | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
OUR TEAM
LAB 2 WRITE-UPBackground InformationSYBR Green Dye
ProcedureSmart Phone Camera Settings
Calibration The camera was placed on a cradle that was in approximately equal height of the fluorimeter. If the cradle and camera needed to be taller in order to be of equal height to the fluorimeter, the cradle was then placed on a stacked glass case until the camera was parallel. The distance from the cradle to the fluorimeter was about 7 cm. After creating a solution for calibration the camera was then set on a self-timer of 10 seconds and then the fluorimeter was encased in a box and covered for complete darkness for the most accurate results. After the beep indicating that the picture was taken the cycle was then complete and the process was then repeated for each solution.
Solutions Used for Calibration
Placing Samples onto the Fluorimeter
Data AnalysisRepresentative Images of Samples [Show an IMAGE where you drew a circle around the droplet with the freehand tool for a sample with no DNA] [Show an IMAGE where you drew a circle around the droplet with the freehand tool for a sample with DNA (positive signal)]
Image J Values for All Samples [See worksheet page 5]
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Fitting a Straight Line
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