BME100 s2014:T Group9 L5: Difference between revisions

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{| style="wikitable" width="700px"
{| style="wikitable" width="700px"
|- valign="top"
|- valign="top"
| [[Image:meandbella.JPG|100px|thumb|Name: Katherine Underwood]]
| [[Image:cassisicoolerthanyou.jpg|100px|thumb|Name: Cassaundra Kinnear<br>]]
| [[Image:BME103student.jpg|100px|thumb|Name: Cassaundra Kinnear]]
| [[Image:meandbella.JPG|100px|thumb|Name: Katherine Underwood<br>]]
| [[Image:BME103student.jpg|100px|thumb|Name: Kyle Queen]]
| [[Image:kylequeener.JPG|100px|thumb|Name: Kyle Queen<br>]]
| [[Image:BME103student.jpg|100px|thumb|Name: Mohammed Binshelail]]
| [[Image:Mohammed's Pic.JPG|100px|thumb|Name: Mohammed Binsheliail<br>]]


|}
|}
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'''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 4s
* Type of Smartphone: iPhone 4s
** Flash:off
** Flash: off
** ISO setting:
** ISO setting: N/A
** White Balance:  
** White Balance: N/A
** Exposure:
** Exposure: N/A
** Saturation:
** Saturation: N/A
** Contrast:
** Contrast: N/A
 
''[Instructions: If you used an additional phone, describe the other type of smart phone you used and how you adjusted the camera settings, if applicable. If not, delete this part]''
* Type of Smartphone:
** Flash:
** ISO setting:
** White Balance:
** Exposure:
** Saturation:
** Contrast:




'''Calibration'''<br>
'''Calibration'''<br>
<br>
The camera was set on a cradle eye level with the sample. We set the camera with a timer so there would be no other light than the LED light the green glow coming from the sample. We clicked the button and closed the flap of the outer black case, then the camera took the picture of the sample.


''[Instructions: Describe how to set up your camera in front of the fluorimeter. Add a PHOTO of this set-up for bonus points.]''
* Distance between the smart phone cradle and drop = 8 cm


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




'''Solutions Used for Calibration''' ''[Instructions: See worksheet page 6.]''
'''Solutions Used for Calibration'''  
{| {{table}} width=700
{| {{table}} width=700
|-
|-
| row 1 cell 1 || row 1 cell 2 || row 1 cell 3 || row 1 cell 4
| Initial Concentration of 2X Calf Thymus DNA solution (micrograms/mL) || Volume of the 2X DNA solution (µL) || Volume of the SYBR GREEN I
Dye solution (µL)
|| Final DNA concentration in SYBR Green I  solution (µg/mL)
|-
| 5 || 80 || 80 || 2.5
|-
| 2 || 80 || 80 || 1
|-
| 1 || 80 || 80 || 0.5
|-
| 0.5 || 80 || 80 || 0.25
|-
|-
| row 2 cell 1 || row 2 cell 2 || row 2 cell 3 || row 2 cell 4
| 0.25 || 80 || 80 || 0.125
|-
|-
| row 3 cell 1 || row 3 cell 2 || row 3 cell 3 || row 3 cell 4
| 0 || 80 || 80 || 0
|}
|}
''[Add more rows as needed]''
 




'''Placing Samples onto the Fluorimeter'''
'''Placing Samples onto the Fluorimeter'''
# ''[Instructions: Step one, in your OWN words]''
# ''Place the fluorimeter into the box''
# ''[Instructions: Step two, in your own words]''
# ''Place the camera in the cradle ''
# ''[Instructions: Step three, in your own words]''
# ''Adjust the height of the fluorimeter with the trays so the camera will see the drop at eye level''
# ''[Instructions: Step etc., in your own words]''
# ''Insert the slide into the fluorimeter''
# ''Adjust the distance between the camera and the slide to be as close as possible without being blury''
# ''Place an 80 microliters drop of SYBR Green in between the first two rows of the slide''
# ''Add 80 microliters of the indicated DNA solution to the drop of SYBR Green''
# ''Align the sample and the blue LED light''
# ''Click the timer on the camera and close the lid for the picture''
# ''Take one more picture, for a total of two pictures, without moving the camera''
 


<br>
<br>
Line 98: Line 105:


==Data Analysis==
==Data Analysis==


'''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]''
[[Image:Droplet_(2).png]]


''[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)]''
[[Image:Droplet_2_(2).png]]




Line 109: Line 117:
'''Image J Values for All Samples'''  
'''Image J Values for All Samples'''  


'''Tube A''' '''Tube B''' '''Tube C''' '''Tube D''' '''Tube E''' '''Tube F''' '''Tube G''' '''Tube H'''
{|
| align="center" style="background:#f0f0f0;"|'''Concentration'''
| align="center" style="background:#f0f0f0;"|'''Area'''
| align="center" style="background:#f0f0f0;"|'''Mean'''
| align="center" style="background:#f0f0f0;"|'''IntDen'''
| align="center" style="background:#f0f0f0;"|'''RawIntDen'''
| align="center" style="background:#f0f0f0;"|'''RawIntDen Back'''
|-
| 0||89824||22.134||1988142||1988142||4075684
|-
| ||106024||25.339||2686504||2686504||3520178
|-
| ||244420||39.829||9735070||9735070||4252614
|-
| 0.25||232620||54.65||12712759||12712759||1470699
|-
| ||213096||60.944||12986996||12986996||1545487
|-
| ||230408||43.885||10111560||10111560||1460134
|-
| 0.5||316088||86.678||27397838||27397838||5561052
|-
| ||263648||111.592||29421095||29421095||5410757
|-
| ||228141||134.47||30678127||30678127||1187005
|-
| 1||275068||121.335||33375368||33375368||1276411
|-
| ||285964||116.944||33441633||33441633||1345189
|-
| ||99532||113.984||11345102||11345102||1352381
|-
| 2||101468||114.739||11642363||11642363||921896
|-
| ||101884||125.741||12810987||12810987||957122
|-
| ||109756||115.55||12682322||12682322||1114350
|-
| 5||108804||173.976||18929237||18929237||654847
|-
| ||109360||120.332||13159480||13159480||796070
|-
| ||106772||111.949||11952999||11952999||918322
|-
|
|}


2308221      14630361
[http://excel2wiki.net/wikipedia.php Excel-to-Wiki Converter].


4078569     


4107249
{|
| align="center" style="background:#f0f0f0;"|'''Tube A'''
| align="center" style="background:#f0f0f0;"|'''Tube B'''
| align="center" style="background:#f0f0f0;"|'''Tube C'''
| align="center" style="background:#f0f0f0;"|'''Tube D'''
| align="center" style="background:#f0f0f0;"|'''Tube E'''
| align="center" style="background:#f0f0f0;"|'''Tube F'''
| align="center" style="background:#f0f0f0;"|'''Tube G'''
| align="center" style="background:#f0f0f0;"|'''Tube H'''
|-
| 2308221||4130155||5069909||5325157||11018266||14630361||17579974||21359877
|-
| 4078569||4773563||5282577||5753055||11153155||16780232||18268541||21671092
|-
| 4107249||5055747||5291947||7644472||13454922||17148850||20260575||22388687
|-
|
|}




''[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.]''
'''Fitting a Straight Line'''<br>
 


TABLE GOES HERE
[[Image:Graph_(2).png]]




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


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



Latest revision as of 09:41, 17 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: Cassaundra Kinnear
Name: Katherine Underwood
Name: Kyle Queen
Name: Mohammed Binsheliail


LAB 5 WRITE-UP

Background Information

SYBR Green Dye

SYBR green dye is used as a nucleic acid stain and binds to DNA. The result is a DNA-dye-complex that absorbs blue light and emits green light. This dye can also bind to single-stranded DNA and RNA with a lower performance.


Single-Drop Fluorimeter

A single-drop fluorimeter is made up of a sturdy black cover used to block out the light. There is a phone cradle used o hold the camera while taking pictures. Inside the black cover there is a platform to hold the slides. There is also an LED light placed around the slides. This light emits a blue light used to see the SYBR green dye.


How the Fluorescence Technique Works

The blue LED light shines on the DNA-dye samples. The amount of DNA in each sample is measured based on the concentration of the green light being emitted from the sample.



Procedure

Smart Phone Camera Settings

  • Type of Smartphone: iPhone 4s
    • Flash: off
    • ISO setting: N/A
    • White Balance: N/A
    • Exposure: N/A
    • Saturation: N/A
    • Contrast: N/A


Calibration

The camera was set on a cradle eye level with the sample. We set the camera with a timer so there would be no other light than the LED light the green glow coming from the sample. We clicked the button and closed the flap of the outer black case, then the camera took the picture of the sample.

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


Solutions Used for Calibration

Initial Concentration of 2X Calf Thymus DNA solution (micrograms/mL) Volume of the 2X DNA solution (µL) Volume of the SYBR GREEN I

Dye solution (µL)

Final DNA concentration in SYBR Green I solution (µg/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 0


Placing Samples onto the Fluorimeter

  1. Place the fluorimeter into the box
  2. Place the camera in the cradle
  3. Adjust the height of the fluorimeter with the trays so the camera will see the drop at eye level
  4. Insert the slide into the fluorimeter
  5. Adjust the distance between the camera and the slide to be as close as possible without being blury
  6. Place an 80 microliters drop of SYBR Green in between the first two rows of the slide
  7. Add 80 microliters of the indicated DNA solution to the drop of SYBR Green
  8. Align the sample and the blue LED light
  9. Click the timer on the camera and close the lid for the picture
  10. Take one more picture, for a total of two pictures, without moving the camera



Data Analysis

Representative Images of Samples


Image J Values for All Samples

Concentration Area Mean IntDen RawIntDen RawIntDen Back
0 89824 22.134 1988142 1988142 4075684
106024 25.339 2686504 2686504 3520178
244420 39.829 9735070 9735070 4252614
0.25 232620 54.65 12712759 12712759 1470699
213096 60.944 12986996 12986996 1545487
230408 43.885 10111560 10111560 1460134
0.5 316088 86.678 27397838 27397838 5561052
263648 111.592 29421095 29421095 5410757
228141 134.47 30678127 30678127 1187005
1 275068 121.335 33375368 33375368 1276411
285964 116.944 33441633 33441633 1345189
99532 113.984 11345102 11345102 1352381
2 101468 114.739 11642363 11642363 921896
101884 125.741 12810987 12810987 957122
109756 115.55 12682322 12682322 1114350
5 108804 173.976 18929237 18929237 654847
109360 120.332 13159480 13159480 796070
106772 111.949 11952999 11952999 918322

Excel-to-Wiki Converter.


Tube A Tube B Tube C Tube D Tube E Tube F Tube G Tube H
2308221 4130155 5069909 5325157 11018266 14630361 17579974 21359877
4078569 4773563 5282577 5753055 11153155 16780232 18268541 21671092
4107249 5055747 5291947 7644472 13454922 17148850 20260575 22388687


Fitting a Straight Line