Z intensity

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Sarah Kefayati Sarah Kefayati
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Z intensity

Search the CONFOCAL archive at http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Hello everyone and hope you all are doing well!
 
 
I am checking the intensity lost along the z axiso f our lenses which are 40x/.8 water dipping lens and 60x/1.2 w lens;by collecting the z stack from a homogeneous fluorescent sample ,I have noticed the max intensity obtained from 60x lens is dropping faster than the 40x dipping lens.I am just wondering this fact is true in general or it's because I'm using a dipping lens?
 
best
Sarah
James Pawley James Pawley
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Re: Z intensity

Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>Hello everyone and hope you all are doing well!
>
>
>I am checking the intensity lost along the z axiso f our lenses
>which are 40x/.8 water dipping lens and 60x/1.2 w lens;by collecting
>the z stack from a homogeneous fluorescent sample ,I have noticed
>the max intensity obtained from 60x lens is dropping faster than the
>40x dipping lens.I am just wondering this fact is true in general or
>it's because I'm using a dipping lens?
>
>best
>Sarah


If your homogenous sample is plastic, then it is unlikely to have the
same RI as the water for which the objectives were designed. Hence
more SA and more signal loss. In the case of the 1.2 lens, you MUST
have a coverslip between the objective and the fluorescent specimen.

If the fluorescent specimen is a water solution, then SA is unlikely
to be the problem and the loss of signal with depth may be related to
the dye concentration being too high and absorbing the excitation
beam as it moves into the specimen.

Jim P.

--
               **********************************************
Prof. James B. Pawley,                          Ph.  608-263-3147
Room 223, Zoology Research Building,              
FAX  608-265-5315
1117 Johnson Ave., Madison, WI, 53706  
[hidden email]
3D Microscopy of Living Cells Course, June 14-26, 2008, UBC, Vancouver Canada
Info: http://www.3dcourse.ubc.ca/             Applications due by March 15, 2008
               "If it ain't diffraction, it must be statistics." Anon.
Julio Vazquez Julio Vazquez
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Re: Z intensity

In reply to this post by Sarah Kefayati
Search the CONFOCAL archive at http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal =
Higher NA lenses are likely to be more sensitive to small differences in coverslip thickness, and/or refractive index mismatch (see for instance: http://www.microscopyu.com/articles/formulas/formulascoverslipcorrection.html ); therefore, under sub-optimal imaging conditions, I would expect the light intensity to drop faster with the 1.2 NA than with the 0.8 NA dipping lens. Also, your 40/0.8 dipping lens may or may not be corrected for a coverslip (check for a "0.17"," "-, or "0" mark)), and either objective may have a correction collar to compensate for differences in coverslip thickness. Whether the setting matches the actual coverslip will also affect the degree of spherical aberration, and therefore the degree of light loss deep in your sample. 


--
Julio Vazquez
Fred Hutchinson Cancer Research Center
Seattle, WA 98109-1024



=

On Feb 7, 2008, at 2:51 PM, Sarah Kefayati wrote:

Search the CONFOCAL archive at http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Hello everyone and hope you all are doing well!
 
 
I am checking the intensity lost along the z axiso f our lenses which are 40x/.8 water dipping lens and 60x/1.2 w lens;by collecting the z stack from a homogeneous fluorescent sample ,I have noticed the max intensity obtained from 60x lens is dropping faster than the 40x dipping lens.I am just wondering this fact is true in general or it's because I'm using a dipping lens?
 
best
Sarah