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Last updated on Mar 2022 

4.4 Laser Configuration Settings 

 

Under 

PMT Setting tab

, click on 

Dye and Detector

. A list of 

commercially available dyes along with its excitation and emission 
values are available for selection.  

1. Choose the appropriate dye. 

2. Select 

Add

.  

3. It will immediately be reflected under phase 1 where each dye 
will be allocated to its respective channel. A transmitted light 
channel will also be shown by default.  

4. Click 

OK

.  

 

Under Laser ND filter: Select 10%.   

 

If you need more than 10% laser power you can switch 
off the ND filter, but most imaging will not need that high 
power of a laser.           

 

Set your laser power for all your channels at 1%.  

 

Emission range could be altered to include a broader range of 
signal otherwise you could use the default settings. 

 

For detectors:  

 

HSD

: keep HV within 350-500. More than 500 will 

produce intense background noise. 

 

SD

:

 keep HV within 600-800. More than 800 will 

contribute to intense background noise. 

Under PMT settings tab: 

 

Mode

: Select 

VBF

 

 

Average

: average a given number of scans to get a 

higher signal to noise ratio.  

 

In 

Line

 

mode

 the averaging will be done on a line-

by-line basis.  

 

In 

Frame mode

 the averaging will be done frame-

by-frame. Drawback: slower scanning time, more 
bleaching, double exposure effect if your sample 
moves. Averaging of 2 times will help you to get 
better quality images if you can afford to do so. 
No averaging or Line averaging is recommended if you are doing live-cell imaging.  

 

Sequential scan: 

Select 

Line

 to prevent crosstalk among the fluorophores. If you select 

None

, simultaneously imaging is done where cross talk is prominent. 

 

 

Confocal Aperture

: press 

Auto

 button to make sure pinhole size is set to optimal 

confocal imaging at Airy Disk ×1. This gives the most optimum size for the thinnest 
optical slice while not sacrificing imaging quality. Increasing the size of the Airy Disk from 

 

Summary of Contents for FV3000

Page 1: ...oking and System Access 4 3 1 Acknowledgements 5 4 Operation Procedures 5 4 1 Switching ON Protocol 5 4 2 Objective lens 6 4 2 Software Initiation 7 4 3 Setting up directory to save images 8 4 4 Laser...

Page 2: ...Immersion Oil Modern immersion oil has no known hazards to human beings so far yet they can cause discomfort to a person if the immersion oil has been left on skin for too long or inhaled Therefore pl...

Page 3: ...taff before they are allowed to access the confocal system 2 1 To arrange a training session Please email Bioimaging Facility bioimaging tll org sg for a training session Fill in the necessary particu...

Page 4: ...er 6pm Sat Sun Public holidays If users require more slots in a particular week they can book on weekdays during non peak hours after 6pm on weekends Sat and Sun and on public holidays If extra time i...

Page 5: ...RT TIMING b Switch on the Master switch on the wall 1 PC 2 Wait until windows icon pops up c Switch on Stage controller box 3 CBH controller 4 d Optional Turn on the Metal Halide lamp 5 if needed e Tu...

Page 6: ...t to 10x objective or lower then click YES Cleaning the stage will take some time b Otherwise click NO to skip cleaning 4 2 Objective lens Objective lens Immersion media 1 25x 0 04 Plan Apochromat Air...

Page 7: ...n the stage mechanism This adds time to the initialization process Do not place anything on the stage mechanism until the initialization process is complete If you are not the first user of the week C...

Page 8: ...y to save all your images Please save in your folder You have several different options on where you can save your images Option 1 D or E Users shaalini create your own folder BPAE cells oir Do keep i...

Page 9: ...oduce intense background noise SD keep HV within 600 800 More than 800 will contribute to intense background noise Under PMT settings tab Mode Select VBF Average average a given number of scans to get...

Page 10: ...to zoom images only in the center Ideal zoom which satisfy the Nyquist limit can be achieved by zooming till the red arrow any zoom beyond it will result in poor resolution and result in more photoble...

Page 11: ...the laser power until red pixels disappear Increase Offset until a dusting of blue pixels in the background are observed Click LSM start to capture an image 4 7 How to do a Z stack for a 3D Image xyz...

Page 12: ...your timelapse experiment Interval FreeRun continues to capture images until it has completed your selected cycle You could always choose an interval of your choice 4 9 Reuse previous settings and ex...

Page 13: ...h the sample and return the stage to central position d Carefully clean the objective lens with Whatman lens tissue using 100 ethanol e Switch lens back to 10x 0 3 objective lens f Exit the FV31S SW s...

Page 14: ...ission please contact Bioimaging Group No stage movement Check the coarse fine movement setting near the focus and xy position knobs It is a physical button that has no electronic indication elsewhere...

Page 15: ...id white or coloured light sometimes red light might be indicative of error III Restart the main controller right at the bottom if none of the steps taken work especially if the machine has been left...

Page 16: ...and cannot be recovered Restart computer terminal Startup popup error code LAST_OPERATION_ NONCOMPLETED The last user did not shut down the program properly or the program encountered a fatal error du...

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