Hi Histonetters,
I work in an animal research facility and we are trying to establish a working
protocol for CISH on bovine tissues.
So far we have tried a Dako PNA ISH kit, and had no luck on bovine tonsil
tissue (have only tried once so far). We have also been trying to optimize the
kit in
Hello All,
I have compiled all of the responses to date regarding the question I posted on
histonet about too much volume and reverse capillary action: (I've changed font
styles to differentiate between responses)
I have used them for quite some time. I was having problems with uneven
their coverplates and the units themselves?
Thanks in advance for your thoughts!
Keri
Keri Colwell, BSc
Laboratory Technologist | Technologiste de laboratoire
TSE and Pathology
Lethbridge Laboratory | Laboratoire de Lethbridge
Canadian Food Inspection Agency | Agence candienne d'inspection des
Hi,
I am currently working on ways to enhance my DAB stiaing and find I am
generating two types of waste that I don't know how to deal with.
One of my techniques involves post-DAB enhancement in a cupric sulfate
solution. My other technique involves making my DAB solution and including
some
for the tetrahydrochloride form, but
again I used the free base and did get some reaction.
Does anyone have thoughts on about how to get the free base to go into
solution without oxidizing, or thoughts about free base versus the other
form of DAB?
Thanks!
Keri
Keri Colwell
Laboratory Technologist