BME103 s2013:T900 Group5 L2

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* 2.) 80 μL of 5μg/mL of calf thymus concentration DNA samples were then added to the slide <br>
* 2.) 80 μL of 5μg/mL of calf thymus concentration DNA samples were then added to the slide <br>
* 3.) To take 3 pictures in the the dark with as much of the blue LED light as possible, we used a timer on the camera, set to 3 seconds. <br>
* 3.) To take 3 pictures in the the dark with as much of the blue LED light as possible, we used a timer on the camera, set to 3 seconds. <br>
-
* 4.) The slide, now containing SYBER Green I and Calf Thymus DNA was then aligned in the cradle such that the light was shining into the DNA. <br>
+
* 4.) The slide, now containing SYBR Green I and Calf Thymus DNA was then aligned in the cradle such that the light was shining into the DNA. <br>
* 5.) With the Camera phone, we captured 3 images of the DNA and removed the light box. <br>
* 5.) With the Camera phone, we captured 3 images of the DNA and removed the light box. <br>
* 6.) That sample was then disposed of with a micropipette <br>
* 6.) That sample was then disposed of with a micropipette <br>
-
* 7.) Repeat with 80μL Green SABR I and 80μL of each Calf Thymus Concentration given by the first column in the table above<br>
+
* 7.) Repeat with 80μL Green SYBR I and 80μL of each Calf Thymus Concentration given by the first column in the table above<br>
==Data Analysis==
==Data Analysis==

Revision as of 12:36, 8 April 2013

BME 103 Spring 2013 Home
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Lab Write-Up 1
Lab Write-Up 2
Lab Write-Up 3
Course Logistics For Instructors
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Image:BME494_Asu_logo.png


Contents

OUR TEAM

Name: Alexander Oropel
Name: Alexander Oropel
Name: Matt McClintock
Name: Matt McClintock
Name: Heewon Park
Name: Heewon Park
Name: Jasmine Joseph
Name: Jasmine Joseph
Name: Cody Gates
Name: Cody Gates
Name: student
Name: student

Cody Gates made 20% contribution to the lab although he may not be noted in the edit history.


LAB 2 WRITE-UP

Background Information

SYBR Green Dye
SYBR Green Dye is a cyanine dye which binds to DNA. The result absorbs blue light and emits a green colored light. This stain works well mostly with double-stranded DNA, but it can still bind to single-stranded DNA. However, it will produce a green fluorescence less effectively with the single-stranded DNA.


Single-Drop Fluorimeter
Image:Fluorimeter.jpg
A single-drop fluorimeter is a type of device that is used to measure patterns of fluorescence in relation to the number of molecules within a medium.


How the Fluorescence Technique Works
The fluorescence technique works by adding a fluorescent die to a liquid with a certain amount of DNA concentration. Teflon coated glass slides were used with a single-drop fluorimeter in order to produce spherical drops on the surface as a result of the hydrophobic properties created by the various circles of uncovered glass.



Procedure

Smart Phone Camera Settings

  • [iphone 4]
    • Flash: Off
    • ISO setting: Auto
    • White Balance: Auto
    • Exposure: Auto
    • Saturation: Auto
    • Contrast: Auto


Calibration
The Camera was set up such that we could get the clearest image with maximum LED light absorption. A light box was placed over the fluorimeter to darken the area. The Smart phone was aligned with the slide to get a sideways picture of the DNA sample. This creates the ideal angle to observe any fluorescent light after the picture is taken. The camera phone is calibrated to view the fluorescent light with little interference from contrast and recording the most light- done by setting the exposure high. The saturation is set to low so that color is not rendered in the photo. The ISO is set to high to maximize focus in the dark setting. With these settings, the fluorescence in the sample is easily observed.


  • Distance between the smart phone cradle and drop = 6.5 cm


Solutions Used for Calibration

Concentration Calf Thymus
(μg/mL)
Volume DNA added
(μL)
Volume SABR GREEN I
(μL)
Concentration resulting DNA
(ng/mL)
5 80 80 2.5
2 80 80 1
1 80 80 0.5
0.5 80 80 0.25
0.25 80 80 .125
0 80 80 blank


Placing Samples onto the Fluorimeter

  • 1.) With the Camera set in place we prepared the slide with SYBR Green I, a constant throughout the experiment
  • 2.) 80 μL of 5μg/mL of calf thymus concentration DNA samples were then added to the slide
  • 3.) To take 3 pictures in the the dark with as much of the blue LED light as possible, we used a timer on the camera, set to 3 seconds.
  • 4.) The slide, now containing SYBR Green I and Calf Thymus DNA was then aligned in the cradle such that the light was shining into the DNA.
  • 5.) With the Camera phone, we captured 3 images of the DNA and removed the light box.
  • 6.) That sample was then disposed of with a micropipette
  • 7.) Repeat with 80μL Green SYBR I and 80μL of each Calf Thymus Concentration given by the first column in the table above

Data Analysis

Representative Images of Samples

no DNA
Image:NoDNA.JPG

with DNA(positive signal)]
Image:DNA10.JPG



Image:Excel.jpg



flotting and fitting a linear graph
Image:Bme103-2.jpg




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