[Histonet] Multiplex IF staining

2016-08-26 Thread Adrienne Anderson via Histonet
Hello Hist-world,
Does anyone have experience doing FISH/double IF staining? My newest project is 
to combine a FISH probe (texas red) with anti-Staufen IF (green secondary) and 
anti-MBNL1 IF (secondary TBD). So I've got a red, green, and blue (DAPI 
counterstain) already. If I used a yellow secondary for the MBNL1, would you be 
able to see the difference between that and the green? I'm running out of 
colors here! Any help would be greatly appreciated.
Thanks so much,Adrienne
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[Histonet] Fixation for FISH

2016-07-22 Thread Adrienne Anderson via Histonet
Hello Histo-land,
I'm going to start doing FISH in our lab, but I've never done it before. I read 
that the PFA fixative solution should be made fresh; however, I have some PFA 
that is being stored in the -80 freezer (for less than a year). Does anyone 
know if this would be ok to use? And actually, if it is ok, I thought about 
making a batch of 3% PFA and aliquoting it into smaller containers to freeze 
and to use at a later time. The only reason I thought about doing that is that 
I've heard to make it can take awhile. But this is all new to me, so any and 
all help would be much appreciated.
I might as well add this as well: specifically, I'll be trying to optimize a 
protocol for Texas red-2-O-methyl-CAG probe with IF for the MBNL1 protein. I've 
read that combining these 2 methods can be trickyand I've never done either 
of them! Is there anyone out there that can give me some advice?
Thanks!Adrienne
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[Histonet] GI Pathologist Consulting

2016-02-01 Thread Adrienne Anderson via Histonet
Hello all,

I was wondering if anyone knows of a GI pathologist interested in doing a quick 
side project as a consultant for the company I work for? If so, please message 
me privately and I can give you the details. 

Thanks so much,
Adrienne Anderson
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