User:Torsten Waldminghaus/flow cytometry notes

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==Use of flow cytometer BD LSR II==
==Use of flow cytometer BD LSR II==
-
*When started new no washing is required but before starting with samples one should press ''''Prime' without any liquid''' (never have 'Prime' with liquid!!!' to let run air run through the system. Than run water on setting "high" on the cytometer.
+
*When started new no washing is required but before starting with samples one should press ''''Prime' without any liquid''' (never have 'Prime' with liquid!!!' to let run air run through the system. Than run water on setting "high" on the cytometer (press 'run').
-
*Start software FACSDiva
+
*Start software FACSDiva:
 +
[[Image:Flow-left.jpg]]
*Select Instrument Configuration  
*Select Instrument Configuration  
**Select presettings of Gunnar F
**Select presettings of Gunnar F
 +
**Press 'Set configuration' and OK
*Go to Cellbiology > Torsten > new exp. (brown icon) > rename (torsten date)>
*Go to Cellbiology > Torsten > new exp. (brown icon) > rename (torsten date)>
*press syringe icon
*press syringe icon
-
*go to 'tube_001' > things will show up on right screen
+
*go to 'tube_001' > things will show up on right screen (Without diagramms shown in picture. Those are set in the following):
-
*make local sheet by pressing on icon on left top
+
[[Image:Flow-right.jpg]]
 +
*make local sheet by pressing on icon beside experiment (left screen)
*Create diagrams:
*Create diagrams:
**Click on DotPlot icon and than on the sheet  
**Click on DotPlot icon and than on the sheet  
-
**Axes can be changed by clicking on the axe-title
+
**Axes can be changed by clicking on the axe-title (right click)
**Make dot plot with FITC versus Hoechst  
**Make dot plot with FITC versus Hoechst  
**Make 4 histograms:
**Make 4 histograms:
Line 39: Line 42:
#Count/FITC
#Count/FITC
#Count/Hoechst
#Count/Hoechst
-
*Go to Instruments > Parameters > Voltage:
+
*Go to Instruments (window on the right of the left screen) > Parameters > Voltage:
**SSC: 500
**SSC: 500
**Hoechst: adjust later using the standart /linear scale
**Hoechst: adjust later using the standart /linear scale
**FITC: 580 /log scale
**FITC: 580 /log scale
*Go to Instruments > Threshhold:
*Go to Instruments > Threshhold:
-
**Press Add two times; delete SSCA and change Hoechst to 5000 for Standard (for samples it should be 2000)
+
**Press 'Add' two times; delete SSC and change Hoechst to 5000 for Standard (for samples it should be 2000)
*Go to laser and set windows ext. to 2000  
*Go to laser and set windows ext. to 2000  
-
*UV delay is 40.000 and can be changed if one gets strange results.
+
*UV delay is 40.000 and can be changed if one gets strange results. (To change, watch the FITC histogramm when delay is changed. The detected FITC should not go down when delay is changed)
'''Recording the standard:'''
'''Recording the standard:'''
*Press "low" at cytometer and insert standard cells  
*Press "low" at cytometer and insert standard cells  
-
*Number of events (number of cells counted) should be adjusted with the smal weel to about 1000-1500 (per second)
+
*In the Aquisition Controls window set the following:
 +
**Storage Gate: All
 +
**Events to record(number of cells counted): 10.000
 +
*Number of events  should be adjusted with the smal weel to about 1000-1500 (per second)
*The dot plot shows two populations: one with FITC staining and one without
*The dot plot shows two populations: one with FITC staining and one without
-
*Lay two windows (vertical) over the dot plot to seperate the two populations
+
*Lay two windows (vertical) over the dot plot to seperate the two populations (The corresponding name will be P1 and P2)
-
*Assign FITC-positive cells to one histogram and FITC-negative to another
+
*Assign FITC-positive cells to one Hoechst-histogram and FITC-negative to the other
*Adjust Hoechst voltage to fit two-chromosome peak of FITC negative cells to channel 60 (make a vertical window with 60 in the middle and monitor the report)
*Adjust Hoechst voltage to fit two-chromosome peak of FITC negative cells to channel 60 (make a vertical window with 60 in the middle and monitor the report)
=> The FITC positive cells show the peak than at about 40 (FITC quenches the Hoechst staining)
=> The FITC positive cells show the peak than at about 40 (FITC quenches the Hoechst staining)

Revision as of 10:03, 22 April 2008

Recipe for flow-TBS

  • 1x TBS with 20mM Tris used for flow cytometry in Skarstad-Lab (reduced NaCl concentration from 150mM in the usual TBS to 130mM (everything else is the same).


1xTBS
for 500 ml
10 ml 1M Tris-HCl pH 7.5
13 ml 5M NaCl
477 ml ddH2O
  • Prepare and sterile filter. Store at 4°C.


Use of flow cytometer BD LSR II

  • When started new no washing is required but before starting with samples one should press 'Prime' without any liquid (never have 'Prime' with liquid!!!' to let run air run through the system. Than run water on setting "high" on the cytometer (press 'run').
  • Start software FACSDiva:

Image:Flow-left.jpg

  • Select Instrument Configuration
    • Select presettings of Gunnar F
    • Press 'Set configuration' and OK
  • Go to Cellbiology > Torsten > new exp. (brown icon) > rename (torsten date)>
  • press syringe icon
  • go to 'tube_001' > things will show up on right screen (Without diagramms shown in picture. Those are set in the following):

Image:Flow-right.jpg

  • make local sheet by pressing on icon beside experiment (left screen)
  • Create diagrams:
    • Click on DotPlot icon and than on the sheet
    • Axes can be changed by clicking on the axe-title (right click)
    • Make dot plot with FITC versus Hoechst
    • Make 4 histograms:
  1. Count/SSCA
  2. Count/Hoechst
  3. Count/FITC
  4. Count/Hoechst
  • Go to Instruments (window on the right of the left screen) > Parameters > Voltage:
    • SSC: 500
    • Hoechst: adjust later using the standart /linear scale
    • FITC: 580 /log scale
  • Go to Instruments > Threshhold:
    • Press 'Add' two times; delete SSC and change Hoechst to 5000 for Standard (for samples it should be 2000)
  • Go to laser and set windows ext. to 2000
  • UV delay is 40.000 and can be changed if one gets strange results. (To change, watch the FITC histogramm when delay is changed. The detected FITC should not go down when delay is changed)

Recording the standard:

  • Press "low" at cytometer and insert standard cells
  • In the Aquisition Controls window set the following:
    • Storage Gate: All
    • Events to record(number of cells counted): 10.000
  • Number of events should be adjusted with the smal weel to about 1000-1500 (per second)
  • The dot plot shows two populations: one with FITC staining and one without
  • Lay two windows (vertical) over the dot plot to seperate the two populations (The corresponding name will be P1 and P2)
  • Assign FITC-positive cells to one Hoechst-histogram and FITC-negative to the other
  • Adjust Hoechst voltage to fit two-chromosome peak of FITC negative cells to channel 60 (make a vertical window with 60 in the middle and monitor the report)

=> The FITC positive cells show the peak than at about 40 (FITC quenches the Hoechst staining)

=> The numbers (volts, channel for - and + FITS) should be written in book

  • Record xxxx events
  • Change Threshhold to 2000 and the Hoechst voltage to move the two chromosome peak to 15 (This is for fast growing cells to not miss high numbers of chromosomes)

=> Write down parameters (FITC+ should be arround 10.5)

  • Record xxxx events

Messure samples:

  • Exchange standard with first sample
  • Click on new sample???? and rename (short name since WinMDI has problems with long names)
  • Watch the event number
  • Move the peak of FITC - cells (standard) to 15
  • Record xxxx events

Save data:

  • Save data as fcs files at K:\Alle\KF_Flow\Montebello\Torsten Waldminghaus\
  • Set the FITC data from log to linear
  • Analyze data with WinMDI
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