Difference between revisions of "Haynes Lab:Notebook/SynBERC Scholars 2013/2014/01/16"

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
 
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|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
 
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{|
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| align="center" style="background:#f0f0f0;"|'''Sample Group'''
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| align="center" style="background:#f0f0f0;"|'''1'''
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| align="center" style="background:#f0f0f0;"|'''2'''
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| align="center" style="background:#f0f0f0;"|'''3'''
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| align="center" style="background:#f0f0f0;"|'''4'''
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| align="center" style="background:#f0f0f0;"|'''5'''
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|-
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| Trial #||||||||||
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|-
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| 1||375909||2014||27168||16339||6393
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|-
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| 2||397251||762||32471||17229||15997
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|-
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| 3||390560||858||29270||13768||17743
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|-
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| AVE||387910||1211||29636||15802||13377
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|-
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| Standard Deviation||10915||696||2670||1797||6111
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|}
  
 
''Notes from Dr. Haynes:''  
 
''Notes from Dr. Haynes:''  
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* Once I get a dsDNA standard, we will create a calibration curve, but first finish measuring these PCR samples.
 
* Once I get a dsDNA standard, we will create a calibration curve, but first finish measuring these PCR samples.
  
 
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"Note by Alfonso and Zazu:"
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*There seemed to be some sort of problem showing the images on the page. They have been uploaded to OWW, but they are not showing on the page.
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*There seemed to be a problem with images 2 and 3 of sample 2. For some reason, they would not enlarge. The quality of the images was also much lower than in December for some reason.
  
  

Latest revision as of 23:38, 26 September 2017

Owwnotebook icon.png Project name Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png

1/16/14

  • Continuation of initial SynBERC expeirment

Sample 1 images have been obtained already.




Part 1: PCR

  • Use the Open PCR machine to amplify segment from "CMV" plasmid DNA
  • Program name = "First Trial 121713"
Reagent 1 2 3 4 5
2x PCR mix 50 50 50 50 50
P0001 1 1 0 0 1
P0002 1 0 1 0 1
DNA template 0.5 0.5 0.5 0.5 0
N.F. H2O 47.5 48.5 48.5 49.5 48
Final vol 100 100 100 100 100

N.F. H2O = nuclease-free water from Promega kit


  1. All components
  2. Forward primer + template DNA
  3. Reverse primer + template DNA
  4. Template DNA only
  5. Primers only


Part 2: Fluorimeter

  • Fluorimeter had to be set up on one 96-hole PCR tube rack + two lids inside the black box
  • Zazu's camera phone was propped up in the black camera cradle with a blue lid from a 50-ml conical tube
  • Today's procedure was as follows:
  1. Diluted 100 uL PCR reactions by adding 500 uL molecular bio grade water (600 uL final volume, 6x dilution)
  2. On hydrophobic slide, applied 80 μL of diluted PCR sample, added 80 uL ready-to-use SYBR green dilution (from DNA day - provided by Dr. Garcia/ Rene Davis)
  3. Did this three times for sample #1 (all components) and sample #2 (forward primer + template DNA). Note: Will continue with other samples after winter break
  4. Zazu used the video function on his iPhone 5: set camera in cradle, started recording, shielded away all light with lid, removed lid, stopped recording. Saved a frame from the movie where light was blocked out as the official image.
  • Image J
  1. Drag & drop image into Image J
  • Cropped image with square selection tool
  • Selected area with circle selection tool
  • Reproduced exact same circle selection in next image by using Edit > Selection > Restore selection
  • Under Analyze > Set Measurements make sure the integrated density option is selected. Click okay.
  • Activate the window of the image you want to measure, hit command-M (or select Analyze > Measure). Window will appear with numbers. Record integrated density in a table or spreadsheet.
  • Repeat this step for next image

image 1 sample 1

image 2 sample 1

image 3 sample 1

image 1 sample 2

image 2 sample 1

image 3 sample 2

image 1 sample 3

image 2 sample 3

image 3 sample 3

image 1 sample 3

image 2 sample 4

image 3 sample 4

image 1 sample 5

image 2 sample 5

image 3 sample 5


Sample Group 1 2 3 4 5
Trial #
1 375909 2014 27168 16339 6393
2 397251 762 32471 17229 15997
3 390560 858 29270 13768 17743
AVE 387910 1211 29636 15802 13377
Standard Deviation 10915 696 2670 1797 6111

Notes from Dr. Haynes:

  • please upload cropped images of the above files and show them here)
  • For the continuation of fluorimeter measurements, image 3 drops for each sample 1 - 5
  • Create a table of integrated density values. Calculate the averages
  • Once I get a dsDNA standard, we will create a calibration curve, but first finish measuring these PCR samples.

"Note by Alfonso and Zazu:"

  • There seemed to be some sort of problem showing the images on the page. They have been uploaded to OWW, but they are not showing on the page.
  • There seemed to be a problem with images 2 and 3 of sample 2. For some reason, they would not enlarge. The quality of the images was also much lower than in December for some reason.