Tom,
We have a few used Bright OTF/AS models available but they are 230v 50
htz so will not suit your region in you are in the USA, if so hopefully
one of our distributors will see your posting.
Please take into account that it is very, very favorable to purchase
from the UK at present.
Best
I use my fingers too, so no help there.
But an automated microtome is great because it frees both hands to
handle a ribbon as it is coming off the blade. It is easy to get
careless if you use a foot pedal but the one time I have been seriously
cut it was with a manual microtome so I guess the
Hi histonetters,
Hope everyone is having a good week so far...
Our hospital receives specimens from a Urology group on a daily basis.
Our PA grosses the specimens here; us histotechs work our magic, and the
hospital pathologists take the slides directly to the Urology office to
read them
Go to http://www.cms.hhs.gov/center/asc.asp for more information about
Ambulatory Surgical Centers (ASC's)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Senn, Amy
R
Sent: Wednesday, January 07, 2009 8:28
Is the histo lab in the urology office CAP certified?
Bernice
Bernice Frederick HTL (ASCP)
Northwestern University
Pathology Core Facility
ECOGPCO-RL
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
I am supposed to try a doublestain using the DAKO autostainer where one of the
antibodies requires a Proteinase K pretreatment and the other antibody requires
antigen retrieval with heat. Should I do both, or will this not work at all?
Thank you
Kimberly C. Tuttle HT (ASCP)
Pathology
Donna
Leica makes a microtome series RM2200 that allows you to cut sections with
the knife guard up. You will be able to decide whether you would like a
rotary microtome or a automated microtome. I see that you like the Leica
CM3050. The comparable microtome for paraffin cutting is the RM2255.
Why does the hospital pathologist go to the Urology to read and sign out
the cases?
So if I am understanding this correctly, your hospital is right now
getting the tech part of the specimen for processing. Is your
pathologist part of the hospital or are they their own group? The
urology group will
The pathologists are probably going to the urology group to read because CLIA
certification is LOCATION specific. The urology group may already have CLIA
cert. and is splitting the interpretation charges with the pathologist. By
adding its own lab, they will be able to capture both tech and
Hi Eva. Here’s how I
would do it.
(1 mole/1064 grams)*(.001 gram/ml)= 9.4 X 10^-7 mole/ml
Concentration 1*Volume 1= Concentration 2 * Volume 2, or
C1V1=C2V2
C1= 9.4 X 10^-7 mole/ml
C2= 10X 10^-9 mole/ml
V2= 2 ml
Solving for V1...
V1= (C2V2)/C1
V1= (10 X 10^-9
Hi Andrea,
It's great to hear that you are happy with your cryostat and, hopefully,
I'll be able to help you with an answer to your question. Leica sells a
small device called a Thermal Block that is designed to help you remove the
specimen from the chuck without causing it to melt. The catalog
Andrea:
I work in a Mohs clinic where all we cut is frozen skin sections. Needless to
say, we don't have 50 chucks laying around... In the morning before clinic
starts we put a layer of freezing medium on chucks and put them in the cryostat
to freeze. When we get specimens, we add another drop
I have the same cyostat, but it doesn't matter which one you use for
removing tissue from the chuck is a separate issue. Others may beg to
differ from my technic, but I remove the block from the cryostat and set it
on a paper towel for a couple of mintes. I do not thaw tissue, just soften
it. I
I guess I wasn't totally clear in my earlier reply. I use my bare fingers but
I also use a camel hair brush as Beth states. I direct the brush with my right
hand and pick up the first part of the ribbon with my left. The brush is used
to hold the last part of the ribbon to aid in maneuvering
Hello Eva
Put simply
1nmol is 10-9 moles
Therefore 10nmol is 10-8 moles
1 mole = 1,064g
Therefore 10-8 moles = 0.1064gor 0.01064mg
Therefore your working solution of 10nmol/ml = 0.01064mg/ml
Your stock solution is 1mg/ml
Therefore your dilution factor is 1.0
Hello Eva
Unfortunately some of the script did not transfer in the original mail and 10-9
should read 10 to the minus 9 as the superscript was lost. The same for 10-8.
Also there should have been a division line between 1.0 and 0.01064 in the
calculation. I hope this helps.
regards
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