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ApoTome2 Quick Guide PDF

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Turn on all power supplies (Sticker No.

1),
wait until TFT fully load

Turn on HBO power box (Sticker No. 2), switch


on ApoTome.2 control Box (Sticker No. 3) and
Turn on the PC (Sticker NO.4). Select Zeiss
user

Press Load Position on TFT to lower the


objectives

Place specimen slide, secure with slide holder

Press
on TFT again for objective back to
working position

2.

3.

4.

5.

8.

Put on a drop of immersion oil on top lens of


63x and 100x oil objective before use

Notes:

In Zen 2011 software, go to Locate tab on left tool


area to examine the specimen on microscope and
identify region of interest
Press Acquisition button to control the microscope
Under Smart Setup, select respective fluorescent
used for the sample with the flexibility of changing
the color according to preference

2.

3.
4.

Double click on ZEN 2011 software icon on desktop


to start the software

1.

Microscope Operation

For further details, kindly contact r.ramupillai@zeiss.com

Turn on Main Switch ( Red labeled A & B)

1.

Switching On the System & Working with Specimen

ApoTome.2 on Axio Imager.Z1 Quick Operating Guide

For optimum image quality, remember to click Min/


Max upon Snap

Leave ApoTome slider OUT for Conventional


Fluorescence Imaging(1) and gently move in ApoTome
Slider manually for Optical Sectioning (2)

Remember to Move the slider out to view image in


software, reminder messages as below, Click OK

For further details, kindly contact r.ramupillai@zeiss.com

8. For Optical Sectioning with ApoTome, move ApoTome slider in manually and set optimum parameter for imaging
capturing under ApoTome Tab before go to Live to preview and proceed with exposure time adjustment and Snap
followed by Min/ Max for every single Channel

7. For Conventional Imaging, Click Snap to capture a 2D Image

6. Adjust Exposure time for every single channel(dye)

5. Go to Live to preview the sample (focus on your sample and do necessary adjustment to achieve best image)

Notes:

For further details, kindly contact r.ramupillai@zeiss.com

ApoTome Settings

For further details, kindly contact r.ramupillai@zeiss.com

3D Imaging Acquisition (Z-Stack Module)

Click Gallery to view all the slices capture with Show Dimension Labels for thickness details

6.

Click on Start Experiment button to start recording of the Z-Stack.

5.

Using focus drive of the microscope to focus on the highest position of the specimen. Click on Set First button to set the highest
position of the Z-stack. Focus in different direction to the lowest position of specimen. Click on the Set Last button to set the
lowest position. Click again on Live button to stop specimen scanning (prevent specimen from bleaching).

3.

Click on the number of slice thickness after Optimal to optimize number of slices to match the optimal Z-interval to the stack
size. Under Optimize Sectioning and step section, choose Optimal button to match the optical section from each channel.

Click on Live button to fast scan the specimen.

2.

4.

Check on checkbox of Z-stack experiment. The Z-Stack Tool bar appears.

1.

For further details, kindly contact r.ramupillai@zeiss.com

1. For 3D Projection, click 3D on the left panel of the Image with various option for 3D view

3D Projection

For 3D Images, go to file and select export option

2.

For further details, kindly contact r.ramupillai@zeiss.com

Go to File, Save or Save as, select the folder and Save type

1.

To Save Images

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