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Selecting an objective 

• 

Open the graphical pop-up menu by clicking on 
the 

Objective

 button (Fig. 10). 

• 

Click on the objective you want to select. The 
selected objective will automatically move into 
the beam path. 

 

Focussing the microscope for transmitted light 

• 

Open the graphical pop-up menu by clicking on 
the 

Transmitted Light

 button (Fig. 11). 

• 

Click on the 

On 

button. Set the intensity of the 

Halogen illuminator using the slider. 

• 

Click on 

Close

 to close the pop-up menu. 

• 

Place specimen on microscope stage. The cover 
slip must be facing up. 

• 

Use the focusing drive of the microscope to 
focus the required object plane. 

• 

Select specimen detail by moving the stage in X 
and Y using the XY stage fine motion control. 

 

Setting the microscope for reflected light 

• 

Click on the 

Reflected Light

 button to open 

the shutter of the HBO 100 mercury lamp. 

• 

Click on the 

Reflector

 button and select the 

desired filter set by clicking on it. 

 

Storing the microscope settings 

Microscope settings can be stored and up to 8 
buttons assigned for fast retrieval and adjustment 
using the 

Microscope Settings 

panel. 

The 

Store

 button permits existing microscope 

configurations to be stored under any name. 

The 

Apply

 button permits existing stored 

microscope configurations to be loaded. 

The 

Delete

 button permits existing microscope 

configurations to be deleted. 

The 

Assign

 button permits the assignment of a 

microscope configuration to a button. 
 

Note:

 

Depending on the microscope 

configuration, settings must be done manually if 
necessary. 

 

Fig. 10 

Microscope Control window, 
e.g.: Axiovert 200 M 

 

Fig. 11 

Microscope Control window with 
Transmitted Light pop-up menu 

Summary of Contents for LSM 510 Inverted

Page 1: ...LSM 510 and LSM 510 META Laser Scanning Microscopes Brief Operating Manual Release 3 5 July 2005...

Page 2: ...e LSM 510 and LSM 510 META laser scanning microscope including its original accessories and compatible accessories from other manufacturers may only be used for the purposes and microscopy techniques...

Page 3: ...nents switch also to ON Now the complete system is ready to be initialized with the LSM Software Switching on the HBO 100 mercury lamp Switch on the HBO 100 mercury lamp via the switch of the power su...

Page 4: ...10 Switchboard window Clicking on this button activates the complete LSM hardware on line mode Click on the Start Expert Mode button in the LSM 510 Switchboard window The LSM 510 Expert Mode Main menu...

Page 5: ...ate toolbar Click on the New button in the File subordinate toolbar The Create New Database window appears Select drive C or D from pull down menu Create a new directory if needed Fig 6 Create New Dat...

Page 6: ...cular tube of the microscope Click on the VIS button to set the microscope for direct observation via the eyepieces of the binocular tube lasers are off Click on the TV button to set the microscope ca...

Page 7: ...ting the microscope for reflected light Click on the Reflected Light button to open the shutter of the HBO 100 mercury lamp Click on the Reflector button and select the desired filter set by clicking...

Page 8: ...ick on the Single Track button in the Configuration Control window Fig 12 Click on the Descanned button if necessary The Beam Path and Channel Assignment panel of the Configuration Control window disp...

Page 9: ...he first line of the Configurations list box and click an Store For loading an existing configuration select it in the list box and click on Apply For deleting an existing configuration select it in t...

Page 10: ...position and diameter When Line button is selected the same rules apply as for Frame Fast Settings Add Track button An additional track is added to the configuration list The maximum of four tracks c...

Page 11: ...lts in the best signal to noise ratio Scan speed 8 usually produces good results Us speed 6 or 7 for superior images Choosing the dynamic range Select the dynamic range 8 or 12 Bit per pixel in the Pi...

Page 12: ...same Optical Size This is important for colocalization studies Image acquisition Once you have set up your parameter as defined in the above section you can acquire a frame image of your specimen Use...

Page 13: ...gh it appears blue on the screen Blue zero minimum Adjusting the laser intensity Set the Pinhole to 1 Airy Unit Fig 21 Set the Detector Gain high When the image is saturated reduce AOTF transmission i...

Page 14: ...upper position of the specimen area where the Z Stack is to start Click on the Mark First button to set the upper position of the Z Stack Then focus on the lower specimen area where the recording of t...

Page 15: ...ing off the system Click on the File button in the Main menu and then click on the Exit button to leave LSM 5 software program Fig 5 If any lasers are still running you should shut them off now in the...

Page 16: ......

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