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Cancer Institute

 

 

Microscopy Core Facility 

 
 

 

V1.0 

Fig 7 – C tab of Multidimensional Acquisition 
 

h)  

Ensure the correct condenser filter is 
selected for application – Fig 8 
 
H – Brightfield 

 

2 – Phase contrast in x20 objective 

 

 

3 – Phase Contrast in x40 and x60      

     

 

      Objectives 

 

 

I,II and III are for DIC applications which are 
not currently installed, treat as brightfield 
 

 

1 is intended for phase contrast using an x10 
objective which is not currently installed 

 
i)  

It is now possible to select the optimal 
settings  for  each  channel  by  clicking 
on  each  channel  separately  and 
selecting  measure  in  the  exposure 
box – This will automatically select an 
optimal exposure time, if you desire a 
known  exposure  time  to  generate  
comparable images select the desired 
exposure 

time. 

The 

Exposure 

Measurement  window  will  open. 
Adjust exposure here or click ok 

 
 
 
 

Figure 8 – Condenser  Controls. 
 
 
 

Condenser 

aperture 

slider 

Condenser 

filter wheel 

Summary of Contents for Axio Imager A1

Page 1: ...sic coverage of use of the Zeiss Axio Imager M1 for multi channelled fluorescent acquisition For more complex usages please contact Fig 1 Front View of Microscope Ocular Viewer Main Stage Mercury Lamp...

Page 2: ...mp control and Microscope power boxes located proximally to main microscope stage Turn on Microscope switch located behind 1st focusing wheel b Turn on computer and Activate AxioVision Program Fig 2 S...

Page 3: ...ieved by pressing stage dropping button and adding a tear sized drop on top of slide so cover slips are necessary and returning stage by pressing stage returning button Make sure at this point to pres...

Page 4: ...u only desire a single multichannel image you can leave out to portions about Z stack Remember to not select a Z stack section f Fig 4 Axiovision Tool Bar a Select Workarea tool bar if workarea is not...

Page 5: ...hannels that will be examined by microscope if chosen For example in the Experiment box shown in Fig 6 the name shown is dapi gfp rhod phase This file will make the microscope acquire images through a...

Page 6: ...1 is intended for phase contrast using an x10 objective which is not currently installed i It is now possible to select the optimal settings for each channel by clicking on each channel separately an...

Page 7: ...begin m Focus to beneath sample and click on stop n Select a slice distance so that z slices are at desired distance from each other o Return Viewing slider to the original position pulled out p Click...

Page 8: ...sample in every channel desired Fig 10 In this format the data is still raw and is best saved to be processed separately afterwards Fig 10 Z stack Window a You can turn each channel collected on and o...

Page 9: ...ocessing option The function of deconvolution is to clean up images to remove positional and chromatic aberrations There are a choice of 3 algorithms which each function in their own way Simply click...

Page 10: ...b select initial and final frame of view desired and enter into parameters section of workarea StartPos and EndPos Fig 12 c Select dimension of view default of ZY d Click Start to create new image Fig...

Page 11: ...ures is not automatically chosen to be the right magnification When you choose to annotate with a scale bar a scaling tab needs to be opened This allows you to set the scale of the image b Select scal...

Page 12: ...age and selecting properties It is in this window that the Attributes tab can be selected where properties of annotations can be changed This is particularly useful when annotation colour is not contr...

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