and the differentiation solution (after the
haematoxylin - if you use it). Check the sections after blueing. If it
looks too weak, increase the Hx staining time /or decrease the
differentiation step. Counterstain with eosin as usual and you should be
right.
Regards
Tony Henwood JP, MSc, BAppSc
visited, as well as several Pathology Colleges (eg CAP and RCPA)
surveys indicate that MOST (if not all) histopathology labs prepare their 10%
formalin fixative from concentrated formalin not polyformaldehyde as you have
incorrectly stated.
Be careful of misinformation.
Regards
Tony Henwood JP
seconds.
9. Counterstain in Metanil Yellow solution, 6 seconds.
10. Rinse in distilled water, 5 seconds.
11. Blot, dehydrate rapidly, clear and mount.
Results:
Fungi stained purple to red against a yellow background.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC
it is
greater than 0.5% formalin
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145
?carbon from lead pensils used for labelling slides.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag
Where is the evidence - or is this another mythical beast some of us
believe?
I don't believe it.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road
lab, they follow
my rules or take a different road. But having said this I will
negotiate, hoping to get the best quality that we can. Communication
(and sometimes education) is the key
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612
Good point
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
My experience is that when you add paraformaldehyde to water all it
forms is a colloidal solution (ie on standing, the paraformaldehyde
settles with very little going into solution (personal experience,
waited one week, then gave up).
Has your experience been different?
Regards
Tony Henwood
What?
Do you roll it in the paraformaldehyde powder?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag
tf wrote:
I DO believe that one reason some people use 4% PFA rather 10% formalin is
that PFA is a bit more stable, both for storage and transportation~~~.
I have not heard this before.
Do you have a reference for this?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC
from paraformaldehyde. If a concentrated
formalin solution (40% formaldehyde) is used, then it should be termed
10% formalin.
If you do a search on Histonet for paraformaldehye, you will find that
this topic has been extensively discussed.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
-Original Message
NINE years ago.
Wow time flys, also God Bless You and check the spelling
Tellnoniczky or Tellyesnicxky,
Oh just give me a beer or Histoclear on the rocks!
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
of placenta, has excess blood been removed from the
placenta? Or have you checked the concentration of formalin (see Jaspers (1987)
J Histotechnol 10 (4): 263-265 for the method using Schiffs reagent).
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior
Only if he is well fixed first!!
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145
From down here in Australia, we hope it goes well.
We are thinking of you.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street
If we don't give it a go, how would we know?
Now I know!!
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Yes,
I would also agree that this would probably be the case.
I have not tried to redo the DAB step after counterstaining,
dehydrating, clearing and mounting.
I would expect it not to work.
Though I could easily be corrected.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC
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