Re: Viability / nuclear stain

From: DAVID JONATHAN NOVO (dnovo@ucla.edu)
Date: Wed Mar 10 1999 - 16:40:03 EST


Hi..

Maybe try going a little "low tech" and have a look at them with trypan
blue under a regular scope. I believe that should give similar results to
PI if everything is going well...

-Dave

On Wed, 10 Mar 1999, Derek Schulze wrote:

> >I have a researcher using PI and AO and they co-stain ALL the cells,
> virtually 100%, in >what they believe to be live samples  of Chondrocytes.
> Any hints?  Does the collagenase >used to break up the matrix of the
> cartilage cause permeabilization?  I'm kind of at a >loss to explain to him
> what is happening.  Any better dye for this application?
> >Any better dye for this application?
> 
> It may not be PI you are seeing.  AO has the unique property of shifting
> its emission to red when at a high enough concentration.  This is often how
> it is used to visualize the transgolgi (I believe).  It accumulates in the
> golgi and after a while turns red.  I guess what I am suggesting is that
> you analyze your samples ASAP as the length of time the samples are exposed
> to the AO will determine how much red you will see.
> 
> Good luck!
> 



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