CONFOCALMICROSCOPY Archives

July 1997

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Richard Thrift <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Tue, 22 Jul 1997 10:18:52 -0800
Content-Type:
text/plain
Parts/Attachments:
text/plain (19 lines)
Hi
I'm interested in trying to correct for bleedthrough by subtracting a
proportion of the green channel signal (based on bleedthrough measured
with only a green label present) from the red channel.

Does this _have_ to be done using the same combination of gain & black
level settings for both images, the image in which bleedthrough is
quantitated, & the image I want to correct?  Is it possible to make this
procedure more useful, so that after measuring bleedthrough at one (or a
few) gain setting(s)for the two channels, I can calculate the correction
required for arbitrary gain settings if e.g. I keep black level constant?  (Is
there a simple relationship between gain and signal?)  I'm using a BioRad
1024, if it matters.

Thanks!
Richard Thrift
DepoTech Corp.
[log in to unmask]

ATOM RSS1 RSS2