RE: sorting bacteria

From: Stefan Andreatta (stefan.andreatta@uibk.ac.at)
Date: Mon Mar 06 2000 - 12:46:53 EST


Jackie,

I am routinely analyzing and sorting very small bacteria (down to 0.2 micron
diameter) from natural water samples using DAPI, Syto13 an other stains.
Usually, I trigger on fluorescence in order not to lose the smaller cells.
This gets more important when sorting, as the drop drive may disturb scatter
signals.

Besides that, we employ a special trigger board on our MoFlo that enables us
to trigger on logarithmically amplified signals and logical combinations
(AND/OR) of different signals. However, measuring quite "large" bacteria
from cultures, should be easily possible without.

For Alignment and counting reference I am using Molecular Probes Alignflow
2.5 micron which are available for 488nm and UV-excitation and 1.0 micron
TransFluoSpheres (also Molecular Probes).

Good luck

Stefan

___________________________________________________________
Stefan Andreatta
University of Innsbruck, Institute of Zoology and Limnology
Technikerstrasse 25, A-6020 Innsbruck, Austria
phone:++43-512-507-6122; fax:++43-512-507-2930
http://zoology.uibk.ac.at/limno/


>
> Dear Flowers,
>
> I will be needing to sort bacteria soon. I've never sorted bacteria before
> so any hints, suggestions,
> advice are welcome. Also, could someone recommend alignment beads for
> bacterial sorting. My
> instrument is a FacsVantage. Thanks in advance for your help.
>
> Jackie Saleh
> Aventis Pharmaceuticals
>
>
>
>



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