We used to put a red bio-hazard bag (the heavy duty one's) into a
cardboard box. This usually did not leak. Just saying if you still
want to use your box method =)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
Hello all and happy long weekend (yes our boss gave us the rest of the
day off at 2!!!)
Looking to stain vasculature in tumors. I did trichrome, pentachrome,
and PAS (with digestion) and am being told that these are not optimal
for what they are looking for. Any other ideas to stain blood
So am getting lots of responses for IHC stains (which is ok), but I am
doing these stains on mouse xenografts and the background is getting in
my way a lot. Was just trying to find a simple special that would do
the trick =)
If IHC is the only way, so be it...was just hoping...
What about
Can you stain for luciferase in tissue?
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
___
Histonet mailing list
Someone just responded “only if it’s possessed”
I laughed =)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
From: Angela Bitting [mailto:akbitt...@geisinger.edu]
Sent: Thursday, June
So I dumped my periodic acid like a moron...does anyone know of another
reagent that will oxidize for the PAS reaction? Looks like I have
acetic and hydrochloric acids...and that is all...hmm...
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
You could have got the tissue wet or to hydrated. Sometimes after you
face the block if you leave it on the ice to long and let moisture get
into the tissue then cut the slide, it looks ok at the time, but once
the moisture gets back out of the tissue it will start to look concave.
If you are
You can also use agar. It does the same thing and is cheaper =)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Just add a little bit more ammonia hydroxide to the water =)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Another solution...get out of clinical and go into research =) There are no
quotas or slide per second expectations in the research world =) So sorry you
are having such a bad time with your job. HT's are not a dime a dozen and
usually it is fairly easy to find a better job. Not to mention
I second this motion!!
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]
Hello all =)
Since I just recently got married and still own a house we do not live
in, I am finding myself in the pickle of 2 houses and not enough
income...Does anyone know of any kind of part time histology jobs in
Austin that I could go to either early until around 7am or late after
5pm? Or
The smoking thing is what I missed...I know I work in cancer research
and I shouldn't smoke, but as I tell everyone...by the time I get lung
cancer I will have helped to find the cure (wishful thinking and stupid
excuse making I know.) Now almost everywhere I work you have to
completely leave the
Quick question...if I am doing PAS (w/o digestion) and not looking for
fungus...would kidney be an appropriate control??
Thanks
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
2035 huh?? Crap!! I won't be retired by then I'll be 54! Hmm...guess
I need to invent the histo. robot so I can still have income!!
=)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
You can buy this type of thing too if you aren't the McGiver type. For
instance...from American Mastertech item # CPW04200E
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original
I'm 30, so blah blah blah...I have 30 or 40 more YEARS!!
=)
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Does anyone have a picture of a positive control Vimentin on human
tonsil? I'm getting some arguments...
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
Ahhh!!! I had this same problem when I came to this lab too!! Plus if
you put that xylene substitute crap (mine was clear rite) it screws up
cell blocks that have been embedded into agar!! 5 experiments had to be
repeated because of this stuff!! The eosin bleed is because you got
water on the
So I just cut a bunch of slides for Ki-7...I am not going to be able to
stain them until Monday. I know the best thing is to put them in 4
degrees, but will it hurt them to stay at room temp for 3 days? Putting
them in the fridge gets a lot of moisture under them and they tend to
lift more. Any
So I am staining tumors that were implanted as cells subdermally into
mice. The cells are human. I am trying to do Caspase staining on these
tumors. The primary is an anti-human rabbit polyclonal, and I am using
a polymer (Biocare Mach3) in lieu of the secondary antibody. The
background is
Usually I think it has to have a door for fire purposes. Especially
since there are so many flammable chemicals in the lab. I could be
wrong?
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
I have had excellent luck and service with them. Call Denise deVines she is
super nice and helpful =)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From:
Does anyone know what the positive control for MET is?
Thanks
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
___
Histonet mailing list
So I have been seeing from this post that people block prior to HIER? I
have always done it as the first step after for 10 minutes (I use the
DAKO enzyme blocker). Is this wrong?
Thanks
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas
This happened to me a couple weeks ago. You got water on the slide
after the eosin staining. Just run it back through alcohols, and rinse
for about five minutes. Change out the alcohols, and re-stain.
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite
You could always get formical which fixes and decals at the same time. This
would eliminate the waiting for fixation. Although I do usually let it fix in
straight formalin overnight first.
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin,
So...I sacrificed a couple of the slides and stained with HE per ya'lls
suggestion and...yay!! Cells all over the place. See I freaked myself
out for nothing. Now, where is 5:00? =)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin,
So I just stained a group of slides all at the same time with the same
conditions. About 40 of 150 the eosin looks like it is bleeding out of
the sections...this has never happened before? What could be the cause
and how do I fix it? Everything is as normal, but again I am being
forced to use
So apparently I'm underpaid =) Good Luck convincing employers of this!
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
The funny part is I hear that can be a fungus control!!
=)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
So I haven't had to deal with rabbit polyclonal primaries in a long time
because I remember how much the background sucks with them.
Unfortunately the only available antibody is a rabbit polyclonal. Does
anyone have any suggestions for how to eliminate the background? I have
diluted almost to
I blocked for all of those...
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: Sebree Linda A [mailto:lseb...@uwhealth.org]
Sent: Tuesday, March 22, 2011 4:13 PM
To:
I just did this last week. I stored them in wash buffer overnight in
the frig. and they were fine =)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From:
I use the Biocare polymers all the time because they are cheaper than
DAKO. Some of them are biotin free, so as long as your primary has no
biotin and you aren't staining anything with endogenous biotin you can
omit that block. Other than that enzyme and protein blocking I still
do. Some of
I actually fixed the cells without the agar overnight, and left them in
the agar overnight...
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: Tony Henwood
Just hack up some spit...
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On
I use the end (without bristles) of a paintbrush
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
So...I am trying to make a cell block using 0.9% agar. I have done this
in the past with no problems. It was at a different facility and I
don't know if the agar is the same? I used bacto-agar this time, but
last week someone tried to do my protocol with agarose and the boogers
dried up and
For the most part you cannot section fat on a cryostat because of the
oilyness (is that a word). You can fix it and section it?
Good Luck
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original
So...I have run down slides and done antigen retrieval on my FFPE
slides. They are currently in antigen retrieval that has come to room
temperature. I am not going to be able to finish the IHC stains until
tomorrow. Will it be better to keep the slides in the antigen retrieval
solution at 4
It's not nice to make fun of people's typing boo-boo's, but thanks for the
Friday chuckle!!
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From:
I personally love polymers!! The DAKO envision is actually using
polymers. You don't have to buy the kit. Biocare has a ton of awesome
polymers for sale that I use in tangent with DAKO. If you want more
specifics on my protocols let me know.
Good Luck
Sarah Goebel, BA, HT(ASCP)
Ahhh!! Everytime I hear those letters I have flash backs to my hospital
days!! Stupid mad cow disease!!
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From:
What?!? A histology lab with no enough space...who ever heard of such a
thing
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
So...trying to find someone who sells RRAS antibody that isn't Abcam. I
can't seem to make the Abcam antibody work and I have been asked to try
and get it from a different company.
2. Does anyone have any experience with RRAS? I have tried dilutions
from 1:500 all the way up to 1:2000. I
Just got to thinking...I do animal tissue processing. I do use an
automated processor, but it is open with no pressure or vacuum. If you
think this will help I can give you the times I use. It is an overnight
process and takes more than a work day worth of hours. Let me know?
Sarah Goebel,
Are you volunteering? That is so nice of you =)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Pathcenters in my opinion don't last as long?
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
At least you have a union!!
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On
I learned from an old school HT and studied using the Carson book. In
this book there are several pages on where to put sections. If you
don't have the Frieda Carson book (or the bible as I refer to it), get
it. A new edition just came out about a year ago. If you're an ASCP
member I think the
You could also try to make them with plasma and thrombin...Unless you
are trying to do IHC with them, it will work fine. The IHC might become
a problem because of the plasma donor's antigens might get in your
way? After you make the booger just fix and it should be fine.
Another way I have tried
Does anyone know of a special or IHC stain to detect chloroform?
Thanks
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
___
Histonet mailing list
I know I have asked about this in the past, but I'm finally getting
around to optimizing my antibody (Caspase3). First, tonsil will be a
good control?
Second, I ordered it from Abcam that is telling me the optimal dilution
is between 1/10 and 1/20. This seems a little crazy? I looked at some
So back at an old job we had an embedding station that had forceps that
plugged in and were constantly hot. Does anyone know where I can just
get the forceps that are always hot? I have the wells in my embedding
center, but it gets frustrating when embedding multiple tiny mouse
tissues and your
I just ordered one from VWR. It's for a thermo tome which I think will
fit on microms? It was $1600. I would call a tech help and see what
they would suggest.
Another thought would be to call IMEB (specifically Denise deVines
18005438496). I have had lots of good luck with the company and
I have always liked paraplast. It's good because you don't seem to have
as much tissue separation from the paraffin in the block. It also seems
to hold up longer on the water bath to give sections a chance to
de-wrinkle themselves without having to pull so much with forceps. It
also doesn't
Of course as most of us would say...histology rocks!! Most histotechs
also do cytology is most hospital settings. The only difference is that
cytotechs actually have to screen the slides that the histo people
prepare. I think that cytologists make slightly more money...but
histology is way more
Hello all,
I am in Austin Texas and would like to know who people use to service
their equipment. I have used Biomed before and wasn't really impressed.
Are there any other companies? The only thing I would really ever need
service on would be the microtome (brand new Thermo 325). I'm just
Look...I am a plethora of questions today!! Has anyone ever used the
antibody Caspase? I hear lymph node is a good positive control, but
where have people purchased the antibody, and at what dilution for FFPE
tissue?
Thanks
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
We always used 95% alcohol to fix, but you're right the blood usually
comes off. Air dry then diff quik (or giemsa) stain works better for a
hema-pathologic stain. You could try Pen Fix (or an alcoholic formalin)
and this might help as opposed to the 95%. Why does the pathologist
need to see
Hey all,
At an old job we had this tiny little blender with a kind of diaphragm
top on it to blend sputum cytology specimens with. It probably only
held about 200cc of fluid at the most. Does anyone have a clue where I
can find one of these?
Thanks
Sarah Goebel, BA, HT(ASCP)
Breathing is my normal way to attack static, it's not a problem getting
the ribbon...there is so much static that when I pull it off the tome,
it literally sucks to my hand like a magnet...and then it's gone.
Thanks everyone for your suggestions! I am hoping to only have to deal
with this for a
I have done this (or tried to do this) as well and almost ended up bald
from ripping out my hair!! My first suggestion would be to try to get
down to a 1/25 or 1/50 dilution. If the background starts to get too
high then try blocking the Fc region. You can buy commercially
available Fc
I think the standard rule of thumb is 700-800 blocks?
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Hello all!!
Hope everyone is gearing up for the festivities of this weekend with
great excitement!!!
Got a quick question. We are going to be using the RRAS antibody and
I'm trying to figure out what a good positive control tissue is. I
looked on the abcam site and it says colon, spleen,
Cutting frozen fat is virtually impossible. There are a few articles I
have seen online (one is called something along the lines of the fat
demon or something pun-tastic like that). Because fat is so oily it
usually doesn't freeze at all. If you have a lot of fat in the tissue
you are trying to
I haven't received anything since Wednesday, but my email is blowing up
now with Histonet stuff! I thought it was just my computer =)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Akemi
Allison
Sent:
Crystals maybe? How cold is the cryostat?
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Thanks Nathan!! I just don't want to be cheated on what I will be
getting paid. My old job is wanting me to come in and do the small
amount of histology work they have. This would all be on evenings and
weekends. It is not PRN, more like call me once a month and I will come
do the work. I'm
How many blocks do you guys normally process before you change the
solutions in the processor?
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
___
What is the going rate for a working histology consultant in Texas? For
instance go in and process, embed, cut, and stain slides when needed?
Thanks
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext.
Hello all!!
I moved jobs, but am still here in 80 degree Austin weather...
Question. If tissue has been stored in 70% alcohol for up to a year,
does there need to be anything done to it before processing? I am
assuming that some rehydration might be necessary? If not can you just
throw it on
Hello all,
Does anyone know what the salary range for a histology supervisor is in
the Austin Texas area?
Thanks
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
-70 or -80 seems a little extreme to me, that's why I always just leave
them in a normal freezer (-20). I think the main point of doing this
from what I understand is so that the antigens stay viable. I know
over time they can degrade and so your stain won't work with some
antibodies. The
Plain slide boxes is ok. I think you can store them for up to a year in
a fridg. (4 degrees), but I usually pu them in a freezer (-20).
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Maybe try handwriting with a pencil then putting the label on aft
erwards.
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
= span style=color: rgb(51, 102, 255);8201 East Riverside Dr.
Bldg 4 Sui= te 100
Austin, Texas 78744
(512)386-2907
American Matertech
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: [Histonet] A Good Human Brain Control
From: Candice Smoots
For the love of your sanity (and keeping your pathologists happy)= DO
NOT BUY A SYMPHONY Their reagents are all proprietary and so
troubleshooting is almost impossible without paying Ventana to have
tech he= lp loom around your lab. The slides take 3 days or so to dry
Do you have a dissecting scope you could use? You can grab one with a
pretty low resolution camera for about $800. If you need more details
let me know.
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
Best decal in the world...Formical-4. It has formalin in it so it fixes
and decals at the same time. You can get plain Jane decal too. The
company is called decal. Here is the website. I think you can also get
it from Fisher?
http://www.decal-bone.com/
Sarah Goebel, B.A., HT (ASCP)
Hey ya'll
I was going through the archives to try and find a solution to this, but
the last post was in 2008, so I thought I would throw it back out there.
I need a human anti human polymer...is there one yet? I looked and
couldn't find one through my normal places.
As to not start the
Roll Roll Roll in the hay =) One of my all time favorite movies!!
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: Re: [Histonet] Un related to actual
Absolutely!! After the buffer rinse (after the counterstain), rinse in
water, then 95, then 100, then xylene, and coverslip away!! I do it
everyday and it works fine =)
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas
Chatter can also be caused by your blade angle. Try making the angle
more obtuse, just don't over do it or you will get venitian (sp?) blind.
The temperature is also a little cold. Try putting your thumb on the
chuck, on top of the tissue, for a few sections before cutting and see
if that helps
I've used this one too, the tip is very tiny, but the pen is awesome!
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: RE: [Histonet] Cassette Marking
What about just a simple old school ski stainer?
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: [Histonet] Plain Vanilla Autostainer?
From: Johnson,
As compared to a lawsuit, yes it's cheaper. But, when trying to explain
to a budget committee that you need something to label things that you
can do by hand...they usually don't see the point. This brings me back
to my original point of mislabelling things 2 times in a year...
Sarah Goebel,
Once upon a time I heard that eosin fluoresces is this true? = ; What
color does it show up? Could this be used as a sort of back gr= ound
stain so you can tell exactly how many cells are in the field?
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
= = XBiotech USA Inc.
I dressed up as Abby from CSI last year. Black wig, bright red
lipstick, and a lab coat is all you need =)
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Actually it's NCIS... =)
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: RE: [Histonet] Un related to actual histology
From: sgoe...@xbiotech.com
Are you wanting to save your specific images, or just need a refe
rence guide for QC? Photobucket or Snapfish are two sites that are
pr= etty cheap if not free?
Sarah Goebel, B.A., HT (ASCP)
Histotec= hnician
XBiotech USA Inc.
= /div
8201 East Riverside= Dr.
Pretty sure you have to run your positive with your negative to keep the
conditions 100% the same. You don't have to put them on the same slide
necessarily, but they need to be on the same run. Also, say you are
running 15 HP patient slides, you can have one negative control for all
of these as
Why do you need a negative control for each block if you are runn= ing
the same antibody on each patient block? Is it just for case by c ase
reference so the negative is filed with the patient slide? Why
co= uldn't you have a control slide bank that was dated so all the
So for every HP you do, you process a control cassette with the patient
tissue cassette? That seems like alot? How do you get that many
control tissues on a daily basis? What do you do with the remaining
tissue in the control block? If you throw them away everyday, I would
be interested in
With one cryostat it is a little bit difficult, but not impossibl= e.
Turn it off at the end of the day (after all the possible frozen s
urgeries are done) and let it defrost overnight. Have someone come
in= an hour or so early to clean it out with 100% alcohol (or formalin
Even with a self-defrosting cryostat, if you are regulated by CAP= you
still have to decontaminate it.
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 E= ast Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-5107
Original
Hey Ya'll,
A friend of mine forwarded me this. We both are HTs and have had to
deal with frozens a lot on a daily basis. Thought everyone might need a
good chuckle on a Monday!!
Cheers!!
http://www.xtranormal.com/watch/6847761/
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
Holy cow man!! Fired for mislabeling 2 times in 260 days!!= nbsp;
Have you never been human and made a mistake?! I could understa= nd
if it was a tech on a regular basis messing up, but that seems a
little = crazy, especially if you are in a high volume hospital!!
What are you needing?
Sarah Goebel, B.A., HT (ASCP)
= Histotechnician
XBiotech USA Inc.
8201 East R= iverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-5107
Original Message
Subject: [Histonet] GLP Compliant Laboratory
From: Karie
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