> From: email@example.com on behalf of Derek Papalegis
> Sent: Wednesday, July 30, 2008 12:52 PM
> To: subat turdi
> Cc: firstname.lastname@example.org
> Subject: Re: Fwd: [Histonet] Processing of mouse hearts
> This is a common problem with mouse tissue. The tissue is being over
> processed. There are a few things that you can do to remedy this. One is
> to have a dedicated processing schedule for each different tissue that
> you process. Although this is ideal, it is often times impossible to
> realistically do this. If your lab is processing a variety of different
> mouse tissues at the same time, you will frequently encounter over
> processed tissue. Although not ideal, a way to get good sections is to
> rough into the blocks and before you put them on your cold tray, place
> them in your heated water bath for a few seconds. This will rehydrate
> the tissue enough so you can get good sections. If you do this often
> enough, you will get a "feel" for how long you need to leave them in
> your water bath.
> It seems like you have a few unnecessary steps in how you prepare these
> hearts. Is there a specific reason why you use cold PBS to rinse the
> blood out of the heart? Wouldn't formalin rinse the blood off just as
> effectively as PBS while also starting the fixation process more
> quickly? What is your reasoning for fixing at 4 degrees instead of at
> room temp? Lowering the temp slows down the fixation process. The 30
> minute running water rinse after fixation is unnecessary as well.
> Feel free to contact me if you have additional questions.
> Derek Papalegis HT (ASCP)
> Division of Laboratory Animal Medicine
> Tufts University
> 136 Harrison Avenue
> Boston, MA 02111
> phone: 617 636-2971
> fax: 617 636-8354
> subat turdi wrote:
> > Folks, I appreciate your responses very much.
> > This is the protocol I use. Please give me some advice what has gone wrong.
> > Animals weighed and anesthetized w/ ketamine-xylazine combo.Chest cavity
> > opened quickly and the heart was exposed. IVC was found and KCl was injected
> > iv to arrest the heart was in diastole.The heart was taken out fast and
> > placed in a cold PBS to wash out the excess blood. (Perfusion w/ PFA through
> > aorta is optional) .The heart was cut into several ~2 mm thick doughnuts
> > with special interest on the ventriculum then put into 4% PFA solution for
> > 24h at 4 degrees.Then the tissue was rinsed with running water for
> > 30min.Then subjected to graded alcohols.
> > 70% 30min
> > 95% 20min X2
> > 100% 20minX2
> > Xylene 20min
> > Xylene 20 min
> > Infiltrate in paraplast:
> > Station 1: 45min
> > Station 2 : 45min
> > Embedding with paraplast
> > My major problem is that a lot of times I get dry blocks. The ribbons i get
> > often comes without the tissue and breaks into shards.
> > Subat
> > On 7/30/08, Gayle Callis wrote:
> >> If you tell us how YOU do it, then we can help modify your protocol.
> >> ----- Original Message ----- From: "subat turdi"
> >> To:
> >> Sent: Tuesday, July 29, 2008 9:31 PM
> >> Subject: [Histonet] Processing of mouse hearts
> >> Dear all,
> >>> Does anyone have a detailed protocol for processing mouse hearts for
> >>> paraffin slides? I am new to this technique and having various troubles in
> >>> getting good histology. We don't have a automatic processer and all is
> >>> manual. Thanks in advance.
> >>> Subat Turdi
> >>> School of Pharmacy
> >>> University of Wyoming
> >>> Laramie, Wyoming
> >>> _______________________________________________
> >>> Histonet mailing list
> >>> Histonet@lists.utsouthwestern.edu
> >>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
> >>> >
> > _______________________________________________
> > Histonet mailing list
> > Histonet@lists.utsouthwestern.edu
> > http://lists.utsouthwestern.edu/mailman/listinfo/histonet
> Histonet mailing list
Histonet mailing list