Reply to: RE>>A clean machine -Reply Sorry group, I should have included in my last message that we use 0.5N NaOH. Happy flowing! Florence -------------------------------------- Date: 2/12/97 3:38 PM To: cyto-inbox From: Maryalice Stetler-Stevenson What is the exact concentration of NaOH? > Reply to: RE>>A clean machine -Reply >We've been using a dilute sodium hydroxide solution to clean the tubing in >our three >FACscans for several years now. We used to use bleach, as recommended by the >manufacturer, and sometimes we would have clogs which never seemed to clear up >completely. Our protein chemist recommended NaOH to me late one afternoon when >I was particularly frustrated with a stubborn clog. The NaOH cleared it right >out, and from then on we've used it regularly to keep the lines clear with few >problems. I've always wondered if anyone else has tried it and how it has >worked for them. >Florence > >-------------------------------------- >Date: 2/11/97 4:21 PM >To: cyto-inbox >From: Jim Zanghi > >>Small beads staying in the instrument can be a problem. Triton X-100 at >>0.1% (the same concentration used to permeabilize cells) in water will >>remove most of them. >> >>Betsy Robertson >>> >>> Running ethanol >>> after the beads seems to help push them through more quickly. >>> >>> Tony Bakke > >I was wondering about what types of solutions can be run through a flow >cytometer without causing damage or corrosion. Is pure ethanol okay? On >the advise of others, I have run 50% hot bleach to clear up clogs, but I >was very weary about doing this since bleach corrodes stainless steel. >I've always followed with a 5 minute water rinse, but this concentration of >bleach seems a bit extreme (we routinely use 10% bleach at room temp). >If 0.1% triton or 70% ethanol is as effective as 50% hot bleach, than this >seems to be the way to go. Any thoughts about this? What do >manufacturers recommend? > >Jim > >-- >James A. Zanghi >Dept. of Chemical Engineering >Northwestern University >Evanston, IL > > > >------------------ RFC822 Header Follows ------------------ >>From flowcyt.cyto.purdue.edu!owner-cyto-sendout Tue Feb 11 14:08:37 1997 >>remote >from donews >Received: from flowcyt.cyto.purdue.edu by donews.cts.com with smtp > (Smail3.1.29.1 #5) id m0vuQNO-00005zC; Tue, 11 Feb 97 14:08 PST >Received: by flowcyt.cyto.purdue.edu (940816.SGI.8.6.9/930416.SGI.AUTO) > for cyto-sendout id MAA10161; Tue, 11 Feb 1997 12:30:01 -0500 >Received: from merle.acns.nwu.edu by flowcyt.cyto.purdue.edu via ESMTP >(940816.SGI.8.6.9/930416.SGI.AUTO) > for <cytometry@flowcyt.cyto.purdue.edu> id LAA09604; Tue, 11 Feb >1997 11:18:55 >-0500 >Received: from [129.105.205.225] (barney.chem-eng.nwu.edu) by >merle.acns.nwu.edu >with SMTP > (1.40.112.8/16.2) id AA138027530; Tue, 11 Feb 1997 10:12:11 -0600 >Message-Id: <v01510103af264a551654@[129.105.205.225]> >Mime-Version: 1.0 >Content-Type: text/plain; charset="us-ascii" >Date: Tue, 11 Feb 1997 10:19:08 -0600 >To: cyto-inbox >From: zanghi@merle.acns.nwu.edu (Jim Zanghi) >Subject: Re: A clean machine -Reply Maryalice Stetler-Stevenson Director Flow Cytometry Unit Laboratory of Pathology, NCI, NIH ------------------ RFC822 Header Follows ------------------ >From box-s.nih.gov!stetler Wed Feb 12 15:07:19 1997 remote from donews Received: from courageous.dcrt.nih.gov by donews.cts.com with smtp (Smail3.1.29.1 #5) id m0vunlm-0000E1C; Wed, 12 Feb 97 15:07 PST Received: from [128.231.220.102] by courageous.dcrt.nih.gov (5.x/Box-1.0) id AA13393; Wed, 12 Feb 1997 18:07:15 -0500 X-Sender: stetler@POserver-s.nih.gov Message-Id: <af27f0100e02100416fc@[128.231.220.102]> Mime-Version: 1.0 Content-Type: text/plain; charset="us-ascii" Date: Wed, 12 Feb 1997 18:09:45 -0400 To: cyto-inbox From: stetler@box-s.nih.gov (Maryalice Stetler-Stevenson) Subject: Re: A clean machine -Reply
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