Fran - You can use Whatman #1 filter paper but it is a lot cheaper and just
as good to use 2 coffee filters. They are the right size for filtering
stains.
Cheryl Crowder
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http
Hello - has anyone used the non-formalin fixative Excell Plus? I have a
researcher who wants to use it. I'm particularly interested in it's
dehydration ability since it is mostly alcohol based. Thank you.
Cheryl Crowder
LSU Ag Center
__
I want to thank those who responded to my inquiry about staining
mycoplasma. The researcher has access to DiffQuik stains in particular and
is going to.try that first. Wish us luck.z
Cheryl Cprowder
___
Histonet mailing list
Histonet@lists.utsouthweste
I work with a researcher who has mycoplasma species cells on agar. He does
not have access to a fluorescent microscope. Does anyone know of a
technique using regular stain?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsout
Charles -
The best control for a non-blood Giemsa stain is a mast cell tumor from a
canine. You can probably get a block from the Univ of Penn Vet School. It
is really close to you. The mast cells will stain purple or magenta.
Cheryl
___
Histonet mai
dyeing
or marking these tissues so I can see them better to embed. Thanks in
advance,
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
ink is permanent there was no problem losing it during processing and the
fine points left just small dots. The only thing is that the tissues should
be blotted well as moisture seems to cause a little bleeding.
Cheryl Crowder, HTL(ASCP
Some years ago the name of cresyl echt violet was changed to cresyl violet
acetate (no CI #). It is what is now used in staining for Nissl substance.
Cheryl Crowder
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http
Hi -
Would the person who contacted me about a used processor please e-mail again.
Thank you.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark Ave.
Baton Rouge, LA 70820
(225) 772-2865
___
Histonet mailing
er initial
fixation with Davidson's (or modified Davidson's), place the eye in 70%
alcohol overnight. There is no need to place the eye in formalin after the
Davidson's fixation.
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark Ave.
Baton Rouge, L
ectronic switch.
Any help any one of you can give me, contact me personally. Thank you in
advance,
Cheryl Crowder, BA, HTL(ASCP)
Animal Science Department
LSU
Baton Rouge, LA 70820
(225) 772-2865
___
Histonet mailin
ink of the PAS.
Cheryl Crowder
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
I am the first to admit I know little to nothing about EM. I have a
researcher who read an article today that said in the method that they had
taken cells, applied them to copper EM grids and immersed them in liquid
nitrogen to fix them. Has anyone ever heard of this technique? and if you
hav
Henk - Mast cells, on tissue and/or cytospins, are pH dependent - 2.0-2.5.
Tissues are usually already fixed in formalin; cytospins can be fixed in
95% alcohol or formalin. I am sending our directions separately. The stain
should less than 5 minutes totally.
Cheryl
_
ours. But many of the fish
we get have been fixed for a week or more and results are really good.
Contact me personally if you need more information.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark Ave.
Baton Rouge, LA 70820
(225)
Sara- We stained many tissues for chromogranin and found that the
Churukian stain worked a lot better than the Grimelius. It double
impregnates the cells with the silver. Directions are in Carson's book,
but if you don't have it, I can send them to you.
Cheryl
Cheryl Crowde
Bret - You can also check the back side of your blade. We wipe the front of
the blade often, but forget about the back. If paraffin builds up on the
blade the sections will stick.
Cheryl
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
Kim - You can use eosin lightly to counterstain the bile stain. The green
will still contrast well.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark Ave.
Baton Rouge, LA 70820
(225) 772-2865
___
Histonet
Hi - The NSH has a terrific coloring book what explains what we do and is
really fun. It's meant for kids but I used to give it to "newbies" in our
area. It cost a dollar I think. But whatever price, it's worth it.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histo
Ally - I have worked with several pathologists who were color-blind -one to
greens; one to blues. As a result we counterstained the GMS with different
colors. A counterstain is just that. It gives a color to secondary tissue
elements. Light greens, hematoxylin, metanil yellow and nuclear fa
An - You didn't mention what cells you were staining, but I assume it's
mast cells. Thionin stains are very pH dependent. For mast cells, the pH
should be 1. At that pH only mast cells stain.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark
If you are processing mammalian tissue, it can be run with your regular
"human' tissues. Rodent tissues are totally different and require shorter
processing times. As long as your animal tissues are grossed at the proper
thickness you should have no trouble.
Cheryl
_
the dye
for a long time. Chemicals, on the other hand, can outdate. Your best bet
is to dispose of them properly.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Crowder Histology Consulting
4952 Alvin Dark Ave.
Baton Rouge, LA 70820
(225) 772-2865
Pamela - We stained copper with Uzman's method, manually. It uses rubeanic
acid (dithiooxamide) solution. The original procedure takes 2 days, but we
were able to modify it to take less time. I can send it to you personally
if you want to try it. Copper shows as a fine black precipitate.
Hi - There are a myriad of decal solutions. You could contact Gayle Callis
- she is an expert and has given workshops on bone and decaling for some
time. We have used her suggestions of 15-20% formic acid for years, with no
detrimental outcomes even for IHC. However, if you don't want to make
Amy - The AFB (Ziehl-Neelsen, Kinyoun's, etc) will stain any acid-fast
bacteria. The Fite's stain is usually considered specific for mycobacteria.
Cheryl
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailm
Laurie - Tru Sigma/Aldrich. I used to get mine from them.
Cheryl
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Hi - I am staining by hand for a research project and am in need of some 30
slide staining racks. If anyone has any that they want to get rid of,
please contact me. I can use multiples so, even if you have only one.
Cheryl
___
Histonet mailing list
Nareen - Vacuoles in brain and rat testes are often caused by the block
being too cold and dry. Try facing off the block and then placing on
melting ice or cold water. This will rehydrate the block and raise the
temperature. Also, cut slowly, particularly the brain. Vacuoles seen to
appear
Rather than use Halt (or other adhesive) in your water bath, have you tried
using charged slides - those used for IHC. Then air-dry or heat dry the
tissues before deparaffinizing. Any water left in the tissue will cause
wash-offs. Do not lower the pH of the silver solution.
Cheryl Crowder
processed
properly, you have a better chance of getting a good section.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-9734
FA
Hi - Got a taker for the directions. Who know?
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-9734
FAX: 225-578-9720
Hi - I'm cleaning out my office and found the procedure manual, timing disc
and notes for the old A/O TP8000 Processor.If for some reason someone
would like these I will mail them to you. Otherwise they are going in the
trash.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technol
don't cut
well, after facing off soak them in Downy for an hour or so. The first
sections should be really good. If you have any questions, contact me
directly.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of
it's a hassle. Also
the ink and light bulb are expensive, but we wouldn't give ours up for
anything.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bert
Thank all of you who answered by question about fixation of chicken embryos.
We have decided to try alcoholic formalin on the early embryos and add
acetic acid to the older ones with calcification of the calvarium. Wish us
luck.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
really appreciated.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-9734
FAX: 225-578-9720
You can use periodic acid to oxidize your tissues as you would for the PAMS
stain. However, this is not the optimal solution when staining fungi. 5%
chromium trioxide used for the GMS can be reused. Since you are doing the
stains manually, as many of us do, this works particularly well. The
Jen - We do T=blue staining almost daily. If you will contact me directly I
will send you our directions. It is a very inexpensive stain, and can be
reused. You will need to pH it often.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of
Hello Histonetters,
The Louisiana Society for Histotechnology is pleased to announce the
26th Annual Symposium/Convention:
"Your Histeaux Surplus Package"
June 12 & 13, 2009
at the
Bourbon Orleans Hotel
717 Orleans St.
New Orleans, LA 70117
www.bourbonorleans.com
The LSH block of r
Hi all - We have a graduate student growing equine epithelial cells in
culture. Money is really short. She
is wondering if there is a regular special stain for these epithelial cells
rather than the more expensive IHC. Any suggestions?
Thank you, Cheryl
Cheryl Crowder, BA, HTL(ASCP
Thanks for the tip. All I'd need to do is lose the tissue too.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-973
Thanks to all of you who have had problems with the Sakura tape. I have
received multiple methods to try to save the sections. When I have tried
several and combined some I will let you all know what happened so maybe I
can help you. Thanks again,
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief
can
it? The pathologists are really upset over these slides as they are for
continuing education and cannot be replaced.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
microns.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Skip Bertman Drive
Baton Rouge, LA 70803
225-578-9734
FAX: 225-578-9720
"scent" of the
softener was too sweet and we hated smelling it. We chose another scent for
the next container. I have no idea why it works, but it does.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinar
tissue. So it's a double edge sword. If we used white cassettes all the
time, the colored paraffin would be great.
Cheryl
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary Medicine
Louisiana State University
Maxim - You sent me an e-mail in August. I replied several times, but the
e-mail did not go through. Is your address complete or is there another I
can use?
Cheryl Crowder, BA, HTL(ASCP)
Chief Technologist
Anatomic Pathology
Department of Pathobiological Sciences
School of Veterinary
48 matches
Mail list logo