Differences

This shows you the differences between two versions of the page.

--- video_tutorials [2014/05/06 11:41] – admin
+++ video_tutorials [2014/06/18 10:02] – admin
@@ Line 8: / Line 8: @@
 Fluorescence and Fluorescence Microscopy explained by [[http://www.ibiology.org/ibioseminars/nico-stuurman-biography.html|Nico Stuurman]] at UCSF.
-{{youtube>iPrZ84kHH2U?large}}
+{{ youtube>iPrZ84kHH2U?large }}
 [[http://www.ibiology.org/ibioseminars/techniques/nico-stuurman-part-1.html]]
@@ Line 14: / Line 14: @@
 ==== Confocal Microscopy ====
+Mark Armitage explains major components of confocal microscopes and their use.
+{{ youtube>BUSZD4IVYSw?large }}
+This video is part of a series of videos. This is the related playlist: [[https://www.youtube.com/playlist?list=PLO0yDSkagDljzI0bdM5m1njrdLdVa80_N]]
+\\
 Nikons website [[http://www.microscopyu.com/articles/confocal/index.html|MicroscopyU.com]] has a very nice course on confocal microscopy.
@@ Line 19: / Line 27: @@
 Confocal Microscopy explained by Kurt Thorn of the Nikon imaging center at UCSF
-{{ youtube>large:1Q5V442V7xI }}
+{{ youtube>1Q5V442V7xI?large }}
 [[http://www.ibiology.org/ibioseminars/techniques/kurt-thorn-part-1.html]]
@@ Line 26: / Line 34: @@
 Kurt Thorn of UCSF talks about two-photon microscopy which uses intense pulsed lasers to image deep into biological samples. It can be used for imaging thick tissue specimens or even imaging inside of live animals.
-{{ youtube>large:CZifB2aQDDM }}
+{{ youtube>CZifB2aQDDM?large }}
 [[http://www.ibiology.org/ibioeducation/taking-courses/two-photon-microscopy.html]]
@@ Line 35: / Line 43: @@
 The lifetime of the fluorophore signal, rather than its intensity, is used to create the image in FLIM. This has the advantage of minimizing the effect of photon scattering in thick layers of sample ([[wp>Fluorescence-lifetime_imaging_microscopy | FLIM]]).
-{{ youtube>large:haE-ejlYPxw }}
+{{ youtube>haE-ejlYPxw?large }}
 [[http://www.ibiology.org/ibioeducation/taking-courses/fluorescence-lifetime-imaging-microscopy.html]]