On Nov 26, 9:36 am, "Haviland, David L" <[email protected]>
wrote:
> As I run a flow core, I also use just plain old 0.9% saline as well, but... I 
> know of other flow cytometry centers that use DI as sheath.   I B.S. you 
> not... For the short duration of laminar flow, the central stream of sample 
> fluid (whatever your cells are in) is centered within the DI sheath.    No 
> one really cares what happens to the cells once past the interrogation point, 
> let alone the waste line.   DI also tends to keep the machines cleaner and a 
> lot less crystallization around the SIP tube.
>
> Pointed question:  Have I made the switch?   Not yet.   I have about 60L of 
> 10X sheath to use up, but a colleague across the way uses DI, and I'm going 
> to switch after that 60L is gone.
>
> David Haviland, PhD
> UTHSC- Houston Stem Cell Flow Center.
>
> ________________________________________
> From: [email protected] 
> [[email protected]] On Behalf Of DK 
> [[email protected]]
> Sent: Wednesday, November 24, 2010 19:11
> To: [email protected]
> Subject: Re: does anybody have a recipe for flow cytometry sheath fluid?
>
> In article 
> <[email protected]>, Mary 
> <[email protected]> wrote:
>
> >Hi All,
> >> the liquid stream (sheath fluid), which carries and aligns the cells
> >> so that they pass single file through the light beam for sensing in
> >> flow cytometers does anybody knowhow to make a DIY sheath fluid? I
> >> thought maybe using 0.9% saline solution would work...amy thoughts?
> >> regards
>
> Pretty much. A simple PBS is what most everyone uses. E.g., here
> is 1X composition:http://www.biosure.com/rpages/solutions.htm
>
> Make it 10X and filter through 0.2 micron and it won't go bad even
> when non-sterile and without preservatives.
>
> DK
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David why do I need to filter sterilise the PBS?
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