From owner-drosophila@net.bio.net Thu Dec 07 22:00:00 1995 Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!elroy.jpl.nasa.gov!swrinde!howland.reston.ans.net!nntp.coast.net!swidir.switch.ch!swsbe6.switch.ch!scsing.switch.ch!news.belwue.de!fu-berlin.de!cs.tu-berlin.de!uni-erlangen.de!lrz-muenchen.de!kue!as-u03-13.ku-eichstaett.de!wws811 From: wws811@as-nwfs-1.ku-eichstaett.de (RONALD GAUGLER) Newsgroups: bionet.drosophila Subject: Re: visualizing GFP under high power Date: Wed, 6 Dec 1995 19:14:26 Organization: KU Eichstaett (FRG) Lines: 18 Message-ID: References: <49vb0h$mjl@vixen.cso.uiuc.edu> NNTP-Posting-Host: as-u03-13.ku-eichstaett.de X-Newsreader: Trumpet for Windows [Version 1.0 Rev Final Beta #10] In article <49vb0h$mjl@vixen.cso.uiuc.edu> a-schmi@ux1.cso.uiuc.edu (schmid aloisia) writes: >From: a-schmi@ux1.cso.uiuc.edu (schmid aloisia) >Subject: visualizing GFP under high power >Date: 4 Dec 1995 17:26:41 GMT >I am trying to take pictures of Drosophila embryos expressing GFP under >high power (100X) on an inverted microscope. I am wondering if other people >have set up video imaging systems for this kind of fluorescent work and >what kind of software do you find works best? What are the advantages >and disadvantages of the various packages? > Thanks! Alice Schmid Hello Drosophila! .