where to
> expect slightly narky, rhetorical responses.
> Best wishes
> Nick
> - Original Message -
> From: "Adam ."
> To: "John Kiernan"
> Cc: "Nicholas David Evans" ,
> histo...@lists.utsouthwestern.edusent: Saturday, 9 January, 2010
> 09:4
How about fluorescent nissl?
2010-01-10
TF
发件人： Nicholas David Evans
发送时间： 2010-01-10 02:16:57
收件人： Adam .
抄送： histonet
主题： Re: [Histonet] Counterstain for fluorescent tissue
Dear Adam,
Thanks very much for the very helpful advice. I guess my real question, which
you're ans
From: "Adam ."
To: "John Kiernan"
Cc: "Nicholas David Evans" ,
histonet@lists.utsouthwestern.edu
Sent: Saturday, 9 January, 2010 09:41:38 GMT -08:00 US/Canada Pacific
Subject: Re: [Histonet] Counterstain for fluorescent tissue
Hi,
The most common counterstains
Hi,
The most common counterstains for fluorescent work is the nuclear
counterstain DAPI, which fluoresces in the UV spectrum. If your
microparticles fluoresce in that wavelength, then you obviously can't use
that but there are a whole host of other nuclear counterstains that
fluoresce in pretty mu
Dear Nick Evans,
First: Say who and where you are, and who is in charge of your experiments
with mice.
Second: Tell your boss to buy two or three histotechnology textbooks (about
$50 each) and allow himself and you and all your colleagues 30 mins paid daily
reading/lunch time.
John Kier
