We do,
It works well
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Principal Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney
Tel: 612 9845 3306
Fax: 612 9845 3318
Pathology Department
the
Hi,
I am in the process of updating the competencies for histotechs and lab
Assistant in our lab.
I will appreciate it, if you guys could share.
Thanks,
Ade
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Hello,
I have a question please. For the AFB Stain, do we put both the
control tissue and the patient on the same slide?
Thanks,
Ade
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Hi,
I have seen this too. I mitigate the problem by making it up in 50 ml
increments and staining them flat. I draw from around the middle of the
Falcon tube I make it up in. It tends to precipitate so you could filter
it. Don't bother re-using the reagent. It's cheap & easy to make up. I
Hi Reuel,
In my experience this is the ORO crystallizing out on the section. I would
first filter your staining solution, then keep your staining times to as
short as you can. Also changing between 37 and room temperatures may be
useful too.
mills
ᐧ
On Wed, Oct 3, 2018 at 8:39 AM Reuel Cornelia
I was wondering if you could help me know why our Oil Red O have some black
snowflakes on our fat tissue hours after staining or after 24 hours more
snowlflakes precipitation occurs. The staining was reference was from Lillie
RD, Ashburn. Please note that our staining works well between two to
I want to order some folders that have space for blocks to go with the
slides. I swear this exists - I remember very clearly bringing it up as a
suggestion at my last job and the pathologist there shutting it down
instantly (he didn't want to be responsible for checking the block against
the slide
