http://confocal-microscopy-list.275.s1.nabble.com/Settings-adjustment-with-depth-for-a-Zeiss-LSM-510-tp6622398p6625600.html
Thanks alot for the help. I admit I wasn't aware of the option being in the
software itself. I'll try and have a look at their preparations myself and
On 26 July 2011 16:37, G. Esteban Fernandez
> The acquisition software (LSM or ZEN) has that function built in, no need
> for a macro. It is called something like "Z brightness correction" and is
> in the Z stack panel.
>
> Software manuals for LSM and ZEN can be found at the Zeiss FTP site here:
> ftp://lsm.zeiss.com/LSM/User_Area/Manuals/
>
> -Esteban
>
> On Tue, Jul 26, 2011 at 7:26 AM, Pedro Almada <
[hidden email]> wrote:
>
>> *****
>> To join, leave or search the confocal microscopy listserv, go to:
>>
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy>> *****
>>
>> Dear listers,
>>
>> Does anyone know of a VBA macro for the Zeiss Meta which allows users to
>> adjust settings such as gain and laser power according to current focus
>> for
>> the Zeiss LSM 510? I am interested in developing this myself but if there
>> is
>> something already made, that would be great...
>>
>> If you are curious what it's for, it's for some of our users who image
>> whole
>> drosophila brains for structural information. Their common complaint is
>> that
>> half-way through their z-stack they loose image brightness until the last
>> slices are barely visible. Clearing methods like Methyl salicilate aren't
>> really adequate for neuronal structure I'm told, which leads me to
>> consider
>> this method.
>>
>> Either way, any information is welcome.
>>
>> Thanks for reading,
>> Cheers,
>> Pedro Almada
>> *
>> *
>> Research and Microscopy Technician
>> Unidade de Imagiologia Celular,
>> *Instituto Gulbenkian de Ciência*
>> Rua da Quinta Grande, 6
>> 2780-156 Oeiras
>>
>> Phone: + 351 214 464 607
>> Ext: 607
>>
>