[Histonet] Fluorescent immunostaining versus IHC
Our immunofluoroescent staining is commonly done with two fluorophores, and
have done it for both confocal and fluorescence microscopy. It isn't
anymore difficult but there are some tricks to the trade, so to speak. We
basically do it the same as IHC, but have noticed, at least with our
antibodies, the primary antibody concentration increases.
We cannot use a fluorophore directly conjugated to FITC for our mouse
frozen sections and apply these antibodies for fluorescence microscopy -
these are murine CD4 FITC or CD8-FITC - we get NO fluorescence. There are
reasons for this. With human kidney biopsies and IFA staining, the
staining is excellent with directly conjugated primaries - IgG-FITC, etc.
although the frozen sections are fixed minimally with cold acetone.
However, one can increase the fluorescence signal a great deal ( and you
want the brightest signal with the least photobleaching you can get) by
using biotinylated primaries then Strepavidin-Alexa dyes OR a purified
antibody followed by a fluorophore conjugated secondary i.e. secondary
conjugated to FITC or RRX or a rhodamine that is crisp, separates nicely
from FITC, and is more resistant to photobleaching.
With our murine CD marker work, we prefer using a primary that is purified
w/secondary antibody-fluorophore or a biotinylated antibody
w/Strepavidin-Alexa dye (488 equivalent to FITC) or Strepavidin-555
(equivalent to Rhodamine). How we combine them for double IFA staining
With any fluorophore conjugated secondary, it is a good idea to spin the
diluted antibody just before applying to section to eliminate protein
aggregates that have fluorophore attached - we refer to this as glowing
One can purchase secondary antibodies from Molecular Probes that are
conjugated to Alexa dyes and we only use secondary antibodies adsorbed to
the species being stained.
You need to be aware of autofluorescence and what causes it - major
culprits are NBF or paraformaldehyde fixation - very annoying and Histonet
abounds with questions on how to get rid of it, not much fun nor always an
We avoid aldehyde fixatives for this reason and use fresh frozen sections
fixed with acetone or acetone/ethyl alcohol mixture. We avoid methanol
with CD markers. Some use paraformaldehyde or other fixtives but that must
be determined with fixation panels.
I have never used a detection kit for IFA work, everything is inhouse
dilutions of secondary antibodies or Strepavidin Alexas. We do not use
Strepavidin conjugated to any FITC or its derivatives, the rhodamines. We
found they did not hold up as well as Alexa conjugates. FITC and FITC
derivatives are fluoresceinated versus the Alexa dyes which are sulphonated
- with the latter being more stable with less photobleaching when excited.
Our technics tend to be rather purist, and we generally leave Tween out of
buffers, although some do use it. All incubations with the fluorophore
conjugates are done in the dark, so if you use an open immunostainer, it
must be covered or do simple manual staining for that portion. We now
coverslip using Molecular Probes Prolong Gold antifade, hard set and ready
Jackson ImmunoResearch has excellent antibodies - get their hard copy
catalog - a wealth of information. Rockland and Southern Biotechnology are
two more antibody sources. Molecular Probes has a wonderful handbook
although huge, but it is very educational and FREE. Many companies
recommend freezing down aliquots of fluorophore conjugates, and their spec
sheets tell how to do this.
This is a good book both IHC and IFA information:
Immunochemistry 2, a practical approach Edited by AP Johnstone and MW
Turner, ISBN# 0 19 963609 5, paperback. Purchased from Springer-Verlag
publishers, they have a website.
very you wrote:
I do confocal microscopy rather than on paraffin sections but I can
tell you this: Try to get a primary conjugated antibody where possible.
The more steps you have, the more steps that can go wrong. It's also
less expensive to get a primary conjugated antibody. Many antibodies
that are made for FACS can also be used for immunofluorescent or
On 09/04/2005, at 3:41 AM, Till, Renee wrote:
> Is there a basic protocol for doing fluorescent IHC on frozen or
> paraffin sections? Is it better to use a primary antibody conjugated
> with FITC or whatever, instead of with the secondary? I never thought
> it> would be such a headache figuring out fluorescence staining on
> sectioned tissues as opposed to cells. Also, do you need to get all the
> separate, or can some of the detections kits be used for fluorescence?
Research Histopathology Supervisor
Veterinary Molecular Biology
Montana State University - Bozeman
PO Box 173610
Bozeman MT 59717-3610
406 994-6367 (lab with voice mail)
406 994-4303 (FAX)
Histonet mailing list
<< Previous Message | Next Message >>