Matthew DelGuidice |
*****
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. ***** List members , my sale is closing tomorrow for an unprecedented offering of Olympus Confocal units and components , this will be the last opportunity to get cutting edge technology for the all-important work that you all do ... at a fraction of the cost ....the link to the sale is below ... http://soldtiger.com/cgi-bin/mndetails.cgi?tigergrp2173 Regards, Matt Matthew J DelGuidice Senior Director Tiger Group – Commercial & Industrial 8991 S 52nd Ave Suite 1 Oak Lawn, IL 60453 P: 708.422.7400| C: 847.460.8312 F: 773.304.2986 [hidden email] www.TigerGroup.com -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of micro Sent: Wednesday, May 10, 2017 10:24 AM To: [hidden email] Subject: Re: measure vacuole and cell volume ***** 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 Lili, There's a lot of extra information that would be useful to us to be able to help you with an answer. Perhaps you could upload an image of a slice to imgur (see the header to this email), and that will provide us with some of that (cell size, tissue/culture type, staining pattern, signal to noise ratio, etc.) Different tools will work with different efficacy depending on the parameters I briefly listed above, but probably using FIJI (FIJI.sc) is the way to go. If you don't have any experience in programming or image processing, it's not going to be quick this first time. If you have the intention to do a similar experiment again and again, it is worth investing the time now to learn how to automate the analysis, even if only partially, as it will save you hours of mind-numbing analysis in the future. Best wishes, Chris ________________________________________ From: Confocal Microscopy List <[hidden email]> on behalf of 张莉莉 <[hidden email]> Sent: Wednesday, May 10, 2017 9:37 AM To: [hidden email] Subject: measure vacuole and cell volume ***** 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 all, I have hundreds of zess confocal z stack images. Now I need to measure the volume of the cell and volume of structures inside the cell. Are there softwares or quick way to do it? Thanks! Best regards, LILI ZHANG |
Free forum by Nabble | Edit this page |