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Nikon A1r Laser Scanning Confocal & 2-Photon Microscope

Nikon A1r Laser Scanning Confocal & 2-Photon Microscope

Nikon A1r Laser Scanning Confocal & 2-Photon Microscope

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iii) “Do Not Stitch” simply places tiles next to each other without processing them<br />

***This type of acquisition WILL NOT give individual images for<br />

each tile***<br />

e) Channels – lambda tab<br />

i) This allows you to switch between optical configurations that require a change<br />

in dichroic, light source, IR laser wavelength, or detectors<br />

f) Order of Experiment<br />

i) The drop down menu is written multiplicatively, the experiment will be<br />

executed in the order of options RIGHT to LEFT<br />

25) Image Window<br />

After the acquisition has finished there are several choices for viewing your data<br />

a) Split channel will show each channel as an individual frame<br />

b) Volume view gives an interactive 3D rendering of your data<br />

c) Tile view displays your Zs as a series of thumbnails<br />

d) Maximum intensity projection takes the brightest pixel at each pixel location in<br />

your Z-stack and displays a single image<br />

<br />

8

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