Michelle Peckham |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Listers We've just upgraded the software on our Zeiss LSM 510 to Zen, and I now have to work out how to set up a macro to: Select about 10-15 cells, and mark their positions (X,Y,Z) Zoom in, set image capture parameters, and rotate cells of interest so they all have the same orientation Place a rectangle (the bleach area) precisely on an specific region of each cell for FRAP Take an image for each cell FRAP the cells one by one Collect images after frap for the next ~2 hours (t/12 is about 30 minutes for fluorescence recovery for my protein of interest) every 5 minutes (I did have a macro that used to do most of this on the old LSM software, although it was an absolute pain to set up!) I will be talking to the Zeiss reps tomorrow, but just wondered if anyone had any advice? Cheers Michelle |
DamirSudar |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Michelle, Writing macros in both AIM and ZEN is a fairly complicated affair and you'd need the license for the Zeiss VBA macro editor which will set you back quite a few dollars. It may well be that Zeiss's MultiTime macro (also not cheap) will actually do what you need and that will do a lot of even more complex things if you get more ambitious later. So when talking with Zeiss, check with them whether MultiTime will do the job. It was developed by Zbi Iwinski from Zeiss USA and Zbi is a great resource for all complex things you might want to do with macros and such. Good luck, - Damir On 8/7/2012 11:24 AM, Michelle Peckham wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Dear Listers > > We've just upgraded the software on our Zeiss LSM 510 to Zen, and I now have to work out how to set up a macro to: > Select about 10-15 cells, and mark their positions (X,Y,Z) > Zoom in, set image capture parameters, and rotate cells of interest so they all have the same orientation > Place a rectangle (the bleach area) precisely on an specific region of each cell for FRAP > Take an image for each cell > FRAP the cells one by one > Collect images after frap for the next ~2 hours (t/12 is about 30 minutes for fluorescence recovery for my protein of interest) every 5 minutes > > (I did have a macro that used to do most of this on the old LSM software, although it was an absolute pain to set up!) > > I will be talking to the Zeiss reps tomorrow, but just wondered if anyone had any advice? > > Cheers > > Michelle -- Damir Sudar - Staff Scientist and Deputy for Technology Lawrence Berkeley Laboratory / Life Sciences Division One Cyclotron Road, MS 977, Berkeley, CA 94720, USA T: 510/486-5346 - F: 510/486-5586 - E: [hidden email] WWW: http://www.lbl.gov/lsd/People_&_Organization/Scientific_Staff_Directory/Sudar_Lab.html |
Terclavers, Sven |
In reply to this post by Michelle Peckham
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Michelle, To run a multi-position experiment combined with the bleaching for FRAP, different frame-orientation/zoom settings, time-lapse etc. , you can use the MTS macro (MultiTime), which can be found in C:\ZEN\Macros. Most probably this was the macro you were using before, however it'll be another version updated for ZEN. With best regards, Sven From: Michelle Peckham <[hidden email]> To: [hidden email] Date: 07.08.12 20:27 Subject: FRAP, multipoint time series for 2 hours using Zen on Zeiss 510 LSM Sent by: Confocal Microscopy List <[hidden email]> ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Listers We've just upgraded the software on our Zeiss LSM 510 to Zen, and I now have to work out how to set up a macro to: Select about 10-15 cells, and mark their positions (X,Y,Z) Zoom in, set image capture parameters, and rotate cells of interest so they all have the same orientation Place a rectangle (the bleach area) precisely on an specific region of each cell for FRAP Take an image for each cell FRAP the cells one by one Collect images after frap for the next ~2 hours (t/12 is about 30 minutes for fluorescence recovery for my protein of interest) every 5 minutes (I did have a macro that used to do most of this on the old LSM software, although it was an absolute pain to set up!) I will be talking to the Zeiss reps tomorrow, but just wondered if anyone had any advice? Cheers Michelle ---------------------------------------- This message is intended for a particular addressee only and may contain business or company secrets. If you have received this email in error, please contact the sender and delete the message immediately. Any use of this email, including saving, publishing, copying, replication or forwarding of the message or the contents is not permitted. |
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