BME100 f2013:W900 Group9 L5: Difference between revisions

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|- valign="top"
| [[Image:AllisonLind.jpg|100px|thumb|Name: [[User: Allison Lind | Allison Lind ]]]]
| [[Image:AllisonLind.jpg|100px|thumb|Name: [[User: Allison Lind | Allison Lind ]]]]
| [[Image:BME103student.jpg|100px|thumb|Name: [[User: Sydney M. Lankford | Sydney M. Lankford ]]]]
| [[Image:Slankford_BME100.jpg|100px|thumb|Name: [[User: Sydney M. Lankford | Sydney M. Lankford ]]]]
| [[Image:Kjw_528_-1600x1200-.jpg|100px|thumb|Name: [[User:Neel J. Patel | Neel J. Patel]] <br> Role: Open PCR Machine Testing <br>]]  
| [[Image:Kjw_528_-1600x1200-.jpg|100px|thumb|Name: [[User:Neel J. Patel | Neel J. Patel]]]]  
| [[Image:BME103student.jpg|100px|thumb|Name: [[User: Callie M. Lamarche | Callie M. LaMarche ]]]]
| [[Image:Callie LaMarche.JPG|100px|thumb|Name: [[User: Callie M. Lamarche | Callie M. LaMarche ]]]]
| [[Image:Julianna A. Brunner.jpg|100px|thumb|Name: [[User:Julianna A. Brunner | Julianna A. Brunner]] <br> Role: Open PCR Machine Testing <br>]]
| [[Image:Julianna A. Brunner.jpg|100px|thumb|Name: [[User:Julianna A. Brunner | Julianna A. Brunner]]]]
|}
|}


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'''SYBR Green Dye'''<br>
'''SYBR Green Dye'''<br>
''[Instructions: A short summary describing SYBR green dye]''<br>
The SYBR green dye has the ability to fluorescence when there is a presence of double-stranded DNA (dsDNA).  According to Life Technologies, SYBR dyes are one of the best high-sensitivity reagents for staining DNA and RNA.  The green dye binds to the DNA, causing the DNA to absorb blue light and reflect green light.
The SYBR green dye has the ability to fluorescene when there is a presence of dsDNA.  


'''Single-Drop Fluorimeter'''<br>
'''Single-Drop Fluorimeter'''<br>
''[Instructions: A description of the single-drop fluorimeter device. Add a PHOTO for bonus points]''<br>
A single-drop fluorimeter device detects PCR-amplified DNA molecules based on the amount of flourescent material in the sample. A blue LED light is shined upon the sample; a camera can then capture green light flourescened by the DNA.
A single-drop fluorimeter device is used to put fluorescene and DNA together on a slide to test for fluoresecene.  
<br>
[[Image:Group9_Fluorimeter.jpg|450px]]


'''How the Fluorescence Technique Works'''<br>
'''How the Fluorescence Technique Works'''<br>  
''[Instructions: In your own words]''
The fluorescence technique works by adding DNA and SYBR Green 1 dye to see how much fluorescence shines through with the picture. The higher the concentration the more fluorescence that should be visual when looking at the light shining through the drop.  This happens because of the blue LED light, which shines onto the sample and excites the dye, causing it to fluorescence green light.  The sample congregates at the glass spots on the slide because the rest of the slide is coated in a highly hydrophobic material.
The fluorescence Technique Works by adding DNA and SYBR Green 1 dye to see how much flourence shines through with the picture. The higher the concentration the more flourence that should be visual when looking at the light shining through the drop.  


<br>
<br>
<!-- Note: Be sure to delete the text in brackets: ''[ ]'' -->


==Procedure==
==Procedure==


'''Smart Phone Camera Settings'''<br>
'''Smart Phone Camera Settings'''<br>
''[Instructions: The type of smart phone you used and how you adjusted the camera settings, if applicable (see worksheet page 4).]''
* Type of Smartphone: iPhone 5
* Type of Smartphone: iPhone 5
** Flash: off
** Flash: off
** ISO setting: auto (could not find option on model used)
** ISO setting: auto (no option on model used)
** White Balance: auto
** White Balance: auto (no option on model used)
** Exposure: auto
** Exposure: auto (no option on model used)
** Saturation: auto
** Saturation: auto (no option on model used)
** Contrast: auto
** Contrast: auto (no option on model used)




'''Calibration'''<br>
'''Calibration'''<br>
 
The phone was placed in the cradle at an appropriate angle to view the slide from the side. The fluorimeter was raised in front of the phone to get the right angle (as if it phone were at eye-level with the slide). The camera was placed 7.5 cm away from the drop to ensure that the drop would be in focus. A light box was placed over the set up to provide darkness to take the picture of the light flowing through the DNA and SYBR Green 1. The fluorescence in the sample was easily seen with higher concentrations of SYBR Green 1.
''[Instructions: Describe how to set up your camera in front of the fluorimeter. Add a PHOTO of this set-up for bonus points.]''
<br>
The phone was placed in the cradle at an appropriate angle to view the slide from the side. The fluorimeter was raised in front of the phone to get the right angle. A light box was placed over the set up to provide darkness to take the picture of the light flowing through the DNA and SYBR Green 1. The flourence in the sample was easily seen with higher concentrations of SYBR Green 1.  
[[Image:Group9_CameraSetup.jpg|450px]]


* Distance between the smart phone cradle and drop = 7.5 cm
* Distance between the smart phone cradle and drop = 7.5 cm
''[Instructions: See worksheet page 6.]''


 
'''Solutions Used for Calibration'''
'''Solutions Used for Calibration''' ''[Instructions: See worksheet page 6.]''
{| {{table}} width=700
{| {{table}} width=700
|-
|-
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'''Placing Samples onto the Fluorimeter'''
'''Placing Samples onto the Fluorimeter'''
# ''[Instructions: Step one, in your OWN words]''
# Attach fresh tip to micropipette and set micropipette to 50 micro-liters
# ''[Instructions: Step two, in your own words]''
# Push micropipette plunger to first stop, and place tip into SYBR Green 1 dye, release plunger
# ''[Instructions: Step three, in your own words]''
# Lift tip out of SYBR Green 1 dye and hover micropipette tip directly between two holes of the fluorimeter slide
# ''[Instructions: Step etc., in your own words]''
# Push plunger down to second stop, allowing dye to release onto the slide
# Repeat steps 1-4 but now with the DNA
# After observing the solution on the fluorimeter, discard the solution
# Push micropipette plunger to first stop, place tip in the solution on the slide, and release plunger
# Repeat step 7 if solution still remains on slide, discard micropipette tip
# Repeat steps 1-8 for remaining DNA, make sure to use each hole on the slide only once


<br>
<br>
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'''Representative Images of Samples'''
'''Representative Images of Samples'''


''[Instructions: Show an IMAGE <u>where you drew a circle around the droplet</u> with the freehand tool for a sample with no DNA]''
'''0.0 μg/mL DNA Concentration Image J Analysis'''
<br><br>
[[Image:0.0 DNA and Data.png|550px]]


''[Instructions: Show an IMAGE <u>where you drew a circle around the droplet</u> with the freehand tool for a sample '''with''' DNA (positive signal)]''
 
'''2.5 μg/mL DNA Concentration Image J Analysis'''
<br><br>
[[Image:Group9_2.5ImageJScreenshot.jpg|550px]]




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'''Image J Values for All Samples'''  
'''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: [http://excel2wiki.net/wikipedia.php 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.]''
{|
 
| align="center" style="background:#f0f0f0;"|'''Calf Thymus DNA Concentration (FINAL), μg/mL'''
 
| align="center" style="background:#f0f0f0;"|'''Image Number'''
TABLE GOES HERE
| align="center" style="background:#f0f0f0;"|'''AREA'''
| align="center" style="background:#f0f0f0;"|'''Mean Pixel Value'''
| align="center" style="background:#f0f0f0;"|'''RAWINTDEN OF THE DROP'''
| align="center" style="background:#f0f0f0;"|'''RAWINTDEN OF THE BACKGROUND'''
|-
| 2.5||image 1||17828||17.006||303179||39188
|-
| 2.5||image 2||20135||41.771||841061||40835
|-
| 2.5||image 3||19078||45.546||868928||43759
|-
| 1||image 1||20575||20.664||425158||40548
|-
| 1||image 2||22096||19.014||420125||49107
|-
| 1||image 3||21896||18.092||396148||46448
|-
| 0.5||image 1||20792||29.294||609079||42845
|-
| 0.5||image 2||21090||29.49||621944||44877
|-
| 0.5||image 3||22716||29.888||678927||46969
|-
| 0.25||image 1||18271||26.316||480825||35867
|-
| 0.25||image 2||17540||23.916||419479||33950
|-
| 0.25||image 3||17392||23.244||404253||34440
|-
| 0.125||image 1||21953||13.737||301576||44788
|-
| 0.125||image 2||18710||9.657||180684||41616
|-
| 0.125||image 3||21953||12.31||270236||47888
|-
| 0||image 1||18376||12.349||226917||40649
|-
| 0||image 2||20532||10.045||206243||37931
|-
| 0||image 3||17009||11.212||190697||36581
|}




'''Fitting a Straight Line'''<br>
'''Fitting a Straight Line'''<br>


''[Instructions: Place an IMAGE of your Excel plot with a line of best fit here. See worksheet page 9]''
[[Image:Group9_CalibrationCurve.jpg|500px]]
 


<br>
<br>
<!-- Note: Be sure to delete the text in brackets: ''[ ]'' -->
<!-- Note: Be sure to delete the text in brackets: ''[ ]'' -->

Latest revision as of 23:44, 12 November 2013

BME 100 Fall 2013 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: Allison Lind
Name: Sydney M. Lankford
Name: Neel J. Patel
Name: Callie M. LaMarche
Name: Julianna A. Brunner


LAB 5 WRITE-UP

Background Information

SYBR Green Dye
The SYBR green dye has the ability to fluorescence when there is a presence of double-stranded DNA (dsDNA). According to Life Technologies, SYBR dyes are one of the best high-sensitivity reagents for staining DNA and RNA. The green dye binds to the DNA, causing the DNA to absorb blue light and reflect green light.

Single-Drop Fluorimeter
A single-drop fluorimeter device detects PCR-amplified DNA molecules based on the amount of flourescent material in the sample. A blue LED light is shined upon the sample; a camera can then capture green light flourescened by the DNA.

How the Fluorescence Technique Works
The fluorescence technique works by adding DNA and SYBR Green 1 dye to see how much fluorescence shines through with the picture. The higher the concentration the more fluorescence that should be visual when looking at the light shining through the drop. This happens because of the blue LED light, which shines onto the sample and excites the dye, causing it to fluorescence green light. The sample congregates at the glass spots on the slide because the rest of the slide is coated in a highly hydrophobic material.


Procedure

Smart Phone Camera Settings

  • Type of Smartphone: iPhone 5
    • Flash: off
    • ISO setting: auto (no option on model used)
    • White Balance: auto (no option on model used)
    • Exposure: auto (no option on model used)
    • Saturation: auto (no option on model used)
    • Contrast: auto (no option on model used)


Calibration
The phone was placed in the cradle at an appropriate angle to view the slide from the side. The fluorimeter was raised in front of the phone to get the right angle (as if it phone were at eye-level with the slide). The camera was placed 7.5 cm away from the drop to ensure that the drop would be in focus. A light box was placed over the set up to provide darkness to take the picture of the light flowing through the DNA and SYBR Green 1. The fluorescence in the sample was easily seen with higher concentrations of SYBR Green 1.

  • Distance between the smart phone cradle and drop = 7.5 cm

Solutions Used for Calibration

Calf Thymus DNA solution Concentration (microg / mL) Volume of the 2X DNA Solution (μL) Volume of the SYBR GREEN I Dye Solution (μL) Final DNA concentration in SYBR Green I Assay (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 0.125
0 80 80 blank


Placing Samples onto the Fluorimeter

  1. Attach fresh tip to micropipette and set micropipette to 50 micro-liters
  2. Push micropipette plunger to first stop, and place tip into SYBR Green 1 dye, release plunger
  3. Lift tip out of SYBR Green 1 dye and hover micropipette tip directly between two holes of the fluorimeter slide
  4. Push plunger down to second stop, allowing dye to release onto the slide
  5. Repeat steps 1-4 but now with the DNA
  6. After observing the solution on the fluorimeter, discard the solution
  7. Push micropipette plunger to first stop, place tip in the solution on the slide, and release plunger
  8. Repeat step 7 if solution still remains on slide, discard micropipette tip
  9. Repeat steps 1-8 for remaining DNA, make sure to use each hole on the slide only once


Data Analysis

Representative Images of Samples

0.0 μg/mL DNA Concentration Image J Analysis


2.5 μg/mL DNA Concentration Image J Analysis


Image J Values for All Samples

Calf Thymus DNA Concentration (FINAL), μg/mL Image Number AREA Mean Pixel Value RAWINTDEN OF THE DROP RAWINTDEN OF THE BACKGROUND
2.5 image 1 17828 17.006 303179 39188
2.5 image 2 20135 41.771 841061 40835
2.5 image 3 19078 45.546 868928 43759
1 image 1 20575 20.664 425158 40548
1 image 2 22096 19.014 420125 49107
1 image 3 21896 18.092 396148 46448
0.5 image 1 20792 29.294 609079 42845
0.5 image 2 21090 29.49 621944 44877
0.5 image 3 22716 29.888 678927 46969
0.25 image 1 18271 26.316 480825 35867
0.25 image 2 17540 23.916 419479 33950
0.25 image 3 17392 23.244 404253 34440
0.125 image 1 21953 13.737 301576 44788
0.125 image 2 18710 9.657 180684 41616
0.125 image 3 21953 12.31 270236 47888
0 image 1 18376 12.349 226917 40649
0 image 2 20532 10.045 206243 37931
0 image 3 17009 11.212 190697 36581


Fitting a Straight Line