User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2012/12/18: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">PcTF Subcloning in E. coli</span>
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">PcTF Subcloning in E. coli</span>
|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>}}
|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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=Date=
=18/12/2012=


'''List title'''
'''RFP Plate Reader Serial Dilution'''
# List items
# Transfer 100 μl of RFP from stock to 100μl DI water. (50% solution)
# Transfer 100 μl of 50% solution to 100 μl DI water. (25% solution)
# Transfer 100 μl of 25% solution to 100 μl DI water. (12.5% solution)
# Transfer 100 μl of 12.5% solution to 100 μl DI water. (6.25% solution)
 
'''Plate Reader'''
* Transfer 50 μl of each solution and a control to the Costar 96 clear bottom black side.
* Here is the software setting:
** Fluorescence
** Endpoint
** Full Plate
** Excitation: 540,  Emission: 600
** Optics: Top
** Gain: AutoScale
** Light Source: Xenon Flash,  Lamp Energy: High
** Read Speed: Normal,  Delay: 100 msec,  Measurements/Data Point: 10
** Read Height: 9.5 mm
* Click OK and then Run the experiment.
* Export the data to an excel file.
* The software will deduce the control data from the sample data
 
'''Result'''
 
 
{| border="1"
! Dilution !! RFP (AU)
|-
|format modifier (not displayed) | 100% ||43125
|-
|format  |50% ||format | 16143
|-
|format  |25% ||format | 7978
|-
|format  |12.5% ||format | 4124
|-
|format  |6.25% ||format | 2718
|}

Latest revision as of 22:20, 26 September 2017

PcTF Subcloning in E. coli Main project page
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18/12/2012

RFP Plate Reader Serial Dilution

  1. Transfer 100 μl of RFP from stock to 100μl DI water. (50% solution)
  2. Transfer 100 μl of 50% solution to 100 μl DI water. (25% solution)
  3. Transfer 100 μl of 25% solution to 100 μl DI water. (12.5% solution)
  4. Transfer 100 μl of 12.5% solution to 100 μl DI water. (6.25% solution)

Plate Reader

  • Transfer 50 μl of each solution and a control to the Costar 96 clear bottom black side.
  • Here is the software setting:
    • Fluorescence
    • Endpoint
    • Full Plate
    • Excitation: 540, Emission: 600
    • Optics: Top
    • Gain: AutoScale
    • Light Source: Xenon Flash, Lamp Energy: High
    • Read Speed: Normal, Delay: 100 msec, Measurements/Data Point: 10
    • Read Height: 9.5 mm
  • Click OK and then Run the experiment.
  • Export the data to an excel file.
  • The software will deduce the control data from the sample data

Result


Dilution RFP (AU)
100% 43125
50% 16143
25% 7978
12.5% 4124
6.25% 2718
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