http://confocal-microscopy-list.275.s1.nabble.com/Rejected-posting-to-CONFOCALMICROSCOPY-LISTS-UMN-EDU-tp6866064p6866106.html
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> Have you optimised you microscope ?? Kohler illumination and so on..??
>
> Tineke Vendrig, ing
> technical engeneer optical microscopy
> Delft University of Technology
> Bionano Science
> Kavli Institute of Nanoscience
> Lorentzweg 1
> 2628LJ Delft
> room F185
> Tel: +31 27 89299
> Fax:+31 15 2781202
> email:
[hidden email]
> mobile phone: 06-34241412
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>
> 2011/10/6 Hanna Sas Nowosielska <
[hidden email]>
>
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>> Dear all,
>>
>> For a couple of months we are struggling with a serious problem with
>> the field illumination in our Olympus Scan^R Scanning station. The
>> image of the specimen, when observed on the computer screen is much
>> darker on one side than on the other. We thought it is the lamp but
>> the lamp is new at properly inserted. Then we tried calibrating the
>> optic fiber, but it didn't help at all. Our third guess was the
>> filters.We checked all of the filters - the coating has lots of
>> small dark spots with biggest concentration of the spots in the middle
>> of the filters, but I am concerned if that can produce uneven
>> illumination of the field so that only one part (let say left corner)
>> is underilluminated? So, I turn to you and your experience: did may
>> anyone have the similar problem? Do you have any suggestion what can
>> be the cause of the problem?
>>
>> Best regards,
>> Hanna
>>
>> --
>> Department of Plant Anatomy and Cytology
>> Faculty of Biology and Environmental Protection
>> University of Silesia
>> Jagiellonska Str. 28
>> 40-032 Katowice
>> Poland
>>
>
>
>
> --
> Tineke Vendrig, ing
> technical engeneer optical microscopy
> Delft University of Technology
> Bionano Science
> Kavli Institute of Nanoscience
> Lorentzweg 1
> 2628LJ Delft
> room F185
> Tel: +31 27 89299
> Fax:+31 15 2781202
> email:
[hidden email]
> mobile phone: 06-34241412
>
Jagiellonska Str. 28