CONFOCALMICROSCOPY Archives

June 2021

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Darran Clements <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Thu, 24 Jun 2021 11:14:56 +0000
Content-Type:
text/plain
Parts/Attachments:
text/plain (1 lines)
*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****

You should be able to do Z stacks with the PFS if you select range rather than top/bottom

Imaging Facility Assistant
Wellcome-MRC  Stem Cell Institute
Jeffrey Cheah Biomedical Centre
Cambridge Biomedical Campus
University of Cambridge
Puddicombe Way
Cambridge
CB2 0AW

[log in to unmask]
01223 760 201






-----Original Message-----
From: Confocal Microscopy List <[log in to unmask]> On Behalf Of Csucs Gabor
Sent: 24 June 2021 12:12
To: [log in to unmask]
Subject: Re: A1R with NIS Elements

*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****

Dear Konstantin,

I you think about it, during a z-stack the PFS needs to be deactivated, otherwise you could not do a Z-stack at all.

Greetings			Gabor



-----Original Message-----
From: Confocal Microscopy List <[log in to unmask]> On Behalf Of Konstantín Levitskiy
Sent: 24 June 2021 13:10
To: [log in to unmask]
Subject: Re: A1R with NIS Elements

*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****

Hi Aryeh.
Sorry but in our A1R+ when we are trying to use z-stack our PFS is automatically deactivated. That's annoying...
Best regards,
Konstantin

-----Mensaje original-----
De: Confocal Microscopy List [mailto:[log in to unmask]] En nombre de Aryeh Weiss Enviado el: jueves, 24 de junio de 2021 8:57
Para: [log in to unmask]
Asunto: A1R with NIS Elements

*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****

We do multipoint timelapse acquisitions in multiwell plates. At each point we acquire a z-stack.
We use the PFS (perfect focus system) for each point, and it works nicely.

However, at the end of the acquisition, we get  a popup window telling us the the various time points cannot be merged because the step, range of the Z series are different. This is a minor annoyance because it means that the time points are saved in separate files. This does not happen if we do the same acquisition with the PFS disabled (but then we risk focus drift).

Is there a way to set the program to merge those files when using the PFS?

Thanks in advance
--aryeh

--
Aryeh Weiss
Faculty of Engineering
Bar Ilan University
Ramat Gan 52900 Israel

Ph:  972-3-5317638
FAX: 972-3-7384051

ATOM RSS1 RSS2