BME103 s2013:T900 Group6 L2: Difference between revisions
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| [[Image:BME103student.jpg|100px|thumb|Name: Dale Franco L. Caagbay - Protocol]] | | [[Image:BME103student.jpg|100px|thumb|Name: Dale Franco L. Caagbay - Protocol]] | ||
| [[Image: | | [[Image:Labtwo.jpg|100px|thumb|Name: Cyril Wassef - Background Information/Data Analysis]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: Emmanuel Casildo - Background Information]] | | [[Image:BME103student.jpg|100px|thumb|Name: Emmanuel Casildo - Background Information]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: | | [[Image:BME103student.jpg|100px|thumb|Name: Israel Brewer]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: student]] | | [[Image:BME103student.jpg|100px|thumb|Name: student]] | ||
| [[Image:BME103student.jpg|100px|thumb|Name: student]] | | [[Image:BME103student.jpg|100px|thumb|Name: student]] | ||
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'''Single-Drop Fluorimeter'''<br> | '''Single-Drop Fluorimeter'''<br> | ||
''The single-drop fluorimeter is a fluorescence-based DNA detection device that aids in bringing to light PCR-Amplified DNA. The DNA sample is placed on a slide upon the machine and shined with a blue LED light. When the light hits the sample, the sample's DNA emits a dim green glow. From there, under a controlled, light-limited environment, a camera (specifically a camera on a phone) can be used to capture the green light.''<br> | ''The single-drop fluorimeter is a fluorescence-based DNA detection device that aids in bringing to light PCR-Amplified DNA. The DNA sample is placed on a slide upon the machine and shined with a blue LED light. When the light hits the sample, the sample's DNA emits a dim green glow. From there, under a controlled, light-limited environment, a camera (specifically a camera on a phone) can be used to capture the green light.''<br> | ||
[[Image:Fluorescent.jpg|400px|]] | |||
'''How the Fluorescence Technique Works'''<br> | '''How the Fluorescence Technique Works'''<br> | ||
'' | ''The overall procedure of the fluorescence technique consisted of an extremely hydrophobic (water-hating) surface. This was used in order to not allow any water to be absorbed during the experiment. The slide atop was coated with an adhesive cover in order to keep the molecules in place during analysis, and keep them a certain distance from the slide at the same time. This being so, it alloweed for the blue LED light to be focused in the drop; causing an increase in intensity which helped create the fluorescent environment. In addition, The SBYR Green dye that was added with the solvent helped form a complex with DNA that preferred to stick to the surface than anywhere else on the Fluorimeter. If a water-soluble dye was used instead, the outcome of the experiment would differ because instead of the green glow, a colorful beam of light would have shown through. | ||
*Note that the group used SYBR Green due to the fact it seemed to be the most eco-friendly." | |||
<br> | <br> | ||
<!-- Note: Be sure to delete the text in brackets: ''[ ]'' --> | <!-- Note: Be sure to delete the text in brackets: ''[ ]'' --> | ||
== | ==Protocol== | ||
'''Materials'''<br> | |||
Glass Slides <br> | |||
Camera Phone <br> | |||
Dark Box <br> | |||
SYBR Green 200mL <br> | |||
Flourimeter <br> | |||
DNA Sample Solution <br> | |||
Micropipette and Tips <br> | |||
Phone Cradle<br> | |||
'''Smart Phone Camera Settings'''<br> | '''Smart Phone Camera Settings'''<br> | ||
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'''Calibration'''<br> | '''Calibration'''<br> | ||
The iPhone was placed in a cradle in a way that made the lens the same height of the fluorimeter. In order to make them the same height, glass platforms were placed to raise the height of the fluorimeter. The distance was around 8 cm. The whole system was placed under the dark box and the pictures were taken. This was repeated for each new solution. | |||
Photo of Fluorimeter | Photo of Fluorimeter | ||
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* Take 80 micro-liters of SYBR Green solution into micropipette | * Take 80 micro-liters of SYBR Green solution into micropipette | ||
* Release all of the 80 micro-liters of SYBR Green fluid onto the slide, then ensure that the beam of light hits the droplet. | * Release all of the 80 micro-liters of SYBR Green fluid onto the slide, then ensure that the beam of light hits the droplet. | ||
* | *With a new plastic micropipette, take another 80 micro-liters of DNA Sample and extract into the SYBR Green droplet. Make sure the drops form a ball and doesn't spread around making individual droplets all over the slide. | ||
*After the photo shoot is complete, calibrate the micropipette to 160 micro-liters and extract all of the sample on the slide. | *In order to see the glow of the SYBR Green with the DNA sample solution, a dark environment must be in place to see the dim green light. Place a box casing over the machine and take multiple pictures of the glowing solution. | ||
*After the photo shoot is complete, and pictures are saved onto the phone, calibrate the micropipette to 160 micro-liters and extract all of the sample on the slide. | |||
*Repeat the same steps for the additional DNA Samples. | *Repeat the same steps for the additional DNA Samples. | ||
* Clean Up Workstation | * Clean Up Workstation | ||
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'''Representative Images of Samples''' | '''Representative Images of Samples''' | ||
''[ | ''[[Image:before.jpg|400px|]]'' | ||
*Sample before DNA was present | |||
''[ | ''[[Image:after.jpg|400px|]]'' | ||
*Sample After DNA was present | |||
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{| {{table}} width=700 | {| {{table}} width=700 | ||
|- | |- | ||
| | | DNA Final Concentration (ng/mL)|| Average Mean|| Average IntDens | ||
|- | |||
| 5 || 106.75 || 4083499 | |||
|- | |||
| 2 || 95.35 || 4017729 | |||
|- | |||
| 1 || 79.58 || 3390288 | |||
|- | |||
| .5|| 54.68 || 2879054 | |||
|- | |- | ||
| | | .25 || 45.90 || 1859347 | ||
|- | |- | ||
| | | 0 || 33.69 || 994680 | ||
|} | |} | ||
'''Fitting a Straight Line'''<br> | '''Fitting a Straight Line'''<br> | ||
''[ | ''[[Image:bmelab2graph.jpg|600px|]]'' | ||
Latest revision as of 11:25, 2 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
ProtocolMaterials Smart Phone Camera Settings
Calibration The iPhone was placed in a cradle in a way that made the lens the same height of the fluorimeter. In order to make them the same height, glass platforms were placed to raise the height of the fluorimeter. The distance was around 8 cm. The whole system was placed under the dark box and the pictures were taken. This was repeated for each new solution. Photo of Fluorimeter
Placing Samples onto the Fluorimeter
Data AnalysisRepresentative Images of Samples
Image J Values for All Samples [See worksheet page 5]
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