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Convallaria (lily of the valley) cross section slide - simplest to 
borrow from your local Zeiss sales rep or service engineer. Basically, 
if an Zeiss LSM or Leica SP# gives a decent image, it passes as far as 
a  Zeiss or Leica service engineer is concerned (unless you are looking 
over their shoulder or better driving the scope and see any issues). 
I've not seen Nikon service work on a confocal, so this test might be 
confocal vendor standard. If you do not have a slide already; bummer 
(might be some lily growing outside that you could harvest). The 
www.carolina.com web site search engine is so incredibly bad, I was 
unable to get a hit just now (amazon.com was no better). You can 
probably find it from other prepared slide companies on the Internet.

Practical parameters:

gain 600 (not that all vendors "600' are the same, or even two PMTs in 
the same scanhead).
offset so that all pixel values are above zero (i.e. no laser light)
12-bit data mode
low laser power (ND filter or AOTF control level ... need to run the 
Argon laser in the "good"power range)
NO AVERAGING (averaging is cheating)
Fastest scan speed available [shortest pixel dwell time] (ideally these 
will be identical on both instruments) ... my thanks to Jonathan Boyd of 
Leica for demonstrating that "faster is better" (SP5, standard scan 
speeds vs resonant scanner, sum images when needed to get same total 
dwell time for each mode).
Same size image format for all instruments, i.e. 2048x2048 pixels
highest performance objective lens available, i.e. plan apo 63x/1.4 NA 
oil, full resolution - by my math 60 nm pixel size for 1.4 NA 
(explanation in previous messages at the listserv).

Note: Zeiss and Nikon oil do not play well together. Need to remove the 
oil from the coverglass, clean the coverglass with 70% ethanol, before 
oiling for the other scope.

George
p.s. I have not acquired any of my Convallaria slides for Sebastian 
Munck's et al PiMP super-resolution calculation method (J Cell Sci 2012, 
PubMed 22357945), but am looking forward to doing so in the future. I 
have been getting very nice results with 30 nm pixel size on both our 
LSM710 and Leica SP5 with 63x/1.4NA, relatively bright initially 
specimens, filter size 1.625 (instead of default of 1.1 which is for 
somewhat larger pixel size), 16-bit output (so I don't have to remember 
where the 32-bit to 16-bit command is located), ~1% photobleaching per 
time point. I find it most useful to have one channel time series per 
LIF or LSM file. My thanks to Sebastian and Glen M for sending me the 
ImageJ plugin.

On 8/13/2012 3:36 PM, Arvydas Matiukas wrote:
> *****
> To join, leave or search the confocal microscopy listserv, go to:
> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
> *****
>
> Dear List,
>
> I am looking for  simple and quick test (and sample) to compare
> acquisition across different confocals. Specifically, to our LSM510
> there was recently added Nikon C2 , and users want to know how
> they compare by few practical parameters, e.g. signal sensitivity,
> spectral bleedthrough, bleaching, and  maybe resolution  .
>
> I am aware of papers by Zucker, Pawley, Cole that describe detail
> evaluation of confocal performance, and even recently measured
> some PSFs. However, I am looking for just simple and quick
> test that would allow direct visual comparison of images (simple
> analysis like getting intensity histogram is fine) acquired on different
> confocals.
>
> Please share your thoughts and/or experience.
>
> Thank you in advance,
> Arvydas
> ***************************
>
>
> Arvydas Matiukas, Ph.D.
> Director of Confocal&Two-Photon Core
> Department of Pharmacology
> SUNY Upstate Medical University
> 766 Irving Ave., WH 3167
> Syracuse, NY 13210
> tel.: 315-464-7997
> fax: 315-464-8014
> email: [log in to unmask]
>
>