Dear All we have a limited fund for buying new automatic microtom. we have got
offer from an agent for model RM3600 histoline company - Italyhave any one
worked befor with such model or any recommendations please
thanks
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Dear all
What is your optimal protocol for processing rabbit and chicken eyes ? and do
you prefer to cut it 2 halfs or inject it with NBF 10% or whole processing is
the best ??
Thanks in advance
Mohamed
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Dear all
what is your optimal clearing time in xelene for prostate and tests of dog
samples (about 0.5 cm) ??is there a need for additional clearing in methyl
benzoat ?
thanks
Mohamed
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Dear allI have submitted a proplem about reprocessing tissue blocks that have
patches of stained areas and unstained pale yellow areas (H stain)!!!,
unfortently the proplem didn't solved yet and i have tried all possible
solutions, increasing processing time and ordered new chemicals from other
Dear all
I have couple quesions please
1- is there a protocol for reprocessing of mice kidney and liver after paraffin
embedding due to insufficient processing time?
2- Is there a formula to add to processing agents as softening agents?
thanks
Mohamed
dear all, i'm facing an issue that trouble us when we process tissue samples of
different organs and cutting them; all organs are ok and spread fine and
somoothly on ater path except for kidney sections (looks wrinkled and curled as
if the praffin fram around it prevent it from spread!!!). i
Hi all
i'm in urgent need for operating
SHANDON LIPSHAW PARAFFIN DISPENSER MODEL 224
how to start using it please in simple stepsthanks in advance
mohamed
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email me for arrangment all advice from you well be appreciated
thanks
Dr. Mohamed abd El Razik
Ass. Lec. of Vet. Histology
Faculty Of Veterinary Medicine
Cairo University - Egypt
http://www.facebook.com/mohamed.abdelrazik.9
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hope that help
Mohamed Abd El razik
Ass. Lec. of Cytology Histology
Faculty of Vet. Med.
cairo University- Egypt
From: Rathborne, Toni trathbo...@somerset-healthcare.com
To: 'Canal, Erica' eca...@hei.org; histonet@lists.utsouthwestern.edu
histonet
dear all on histonet
I'm going to setup a new histology lab. in Egypt. I need to contact with you to
advice me about the best and comfotable facilities
microtomes- processors-automatic stainers and so on .
Mohamed
Ass. Lec. of histology
Faculty of Vet. Med.
Cairo University
Egypt
I think these granules are of insoluble hematoxylin or preceptated
hematoxylin granules
a had these condition 2 years ago and resolved it by prepairing new one.
hope these could help
Mohamed Abd el Razik
Ass. Lec. of veterinary histology
Cairo University- Egypt
http://blog.ergle.org/wp-content/plugins/extended-comment-options/markehjf.htm
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dear all
what conference do you recommend in histology and histotechnology feild do you
prefer?
please provide me with date and a link if avaliable
thanx
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hi all
i'm going to apply for PhD degree in using educational technology in Histology
teaching.
do you know any university i could contact for acceptance letter? i have my
funded scholarship
thanx
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thanx to all kind replays from sgoebel, Paula Pierce and JR R.
but i know that Alcian blue 2.5 stain most acidic mucins and pH 1 stain
sulfated one. my quistion is: i found in several serial section on intestine
that 100 goblet cell react to AB ph 1 and only 50 cell reacts to AB 2.5
why??
i have posted my quistion 2-3 times several days ago and recieve no negative or
positive comment !!! why??
is my quistion not clear or what??
--- On Thu, 6/2/11, mohamed abd el razik k8...@yahoo.com wrote:
From: mohamed abd el razik k8...@yahoo.com
Subject: Alcian blue quistion
To: histonet
hi every body
i have a confusing quistion reagrding Alcian blue pH 1 2.5 stains.
suppose you have 100 goblet cell react positive to pH 1 which mean all have
sulfated mucin. and 50 cell from other section react positive to pH 2.5 which
mean acidic type(sulfated or sialated). why these
hi every body
i have a confusing quistion reagrding Alcian blue pH 1 2.5 stains.
suppose you have 100 goblet cell react positive to pH 1 which mean all have
sulfated mucin. and 50 cell from other section react positive to pH 2.5 which
mean acidic type(sulfated or sialated). why these 50 cell
dear all
i'm looking for vendors or companies that we could order some anti chicken
antibodies (primary secondary). speacially for CD4 CD8
i'm new in that feild and need your help.
mohamed
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hi all
i miss you several days.
we are medium research lab and looking forward to bring scanning transmission
electron microscope . so which manufacture or brand and model you recommend us
and average price ??
any offers are welcomed to my mail
thanx in advance
mohamed
---
dear all
can you share me pituitary stain protocol called
PAS/ celestine blue / Orange G?
thanks in advance
mohamed
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dear all
i'm going to detect alkaline phsphatase in avian intestine and i didn't do that
befor so any help with protocol?? or kits for that and how to use it
can we detect it in FFPT?
by the way i have sent a question twice befor about how to diff. between red
muscle and white one and have
Dear all
how can i differentiate between Red Muscle and white one (formalin fixed)?
would you mind to share your protocol
thanx
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Dear all
how can i differentiate between Red Muscle and white one (formalin fixed)?
would you mind to share your protocol
thanx
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i think that histonet is a primary educational group for all levels and any
expert in our feild have asked these quistions one day befor and we should ask
freely without any shame .
i'm as begainner have learned alot from these little quistions.
and i asked befor for name of antibodies and its
cert. to work as i have master degree??
if yes i have searched there site but can't find where i can pass the exams in
Egypt!!
can you send me a link if you reached it ortell me how to be certified if i'm
in Egypt??
thanx in advance
Mohamed Abd El Razik
Histology Dep.
Faculty of Vet. Med.
Cairo
Dear histonetters
i have a requist for all of you as i'm new in histochemistery and IHC as many
other frinds i know in histonet . we found it difficult to know the name and
use of many antibodies in many many topics so we can't understand the all
masages and replaing on it. and lose the
hi all
i'm going to stain some slides of small intestin which were fixed in susa.
i'm going to stain it by Massons trichrome.
i have read that slides should be secondry fixed in Bouin's or saturated picric
solution.
does it mean fixation of processed tissue after cutting with microtom??
how
we are going to bring new one too for our small lab. any suggestion please.
you can send me at k8...@yahoo.com
--- On Wed, 6/30/10, Webb, Dorothy L dorothy.l.w...@healthpartners.com wrote:
From: Webb, Dorothy L dorothy.l.w...@healthpartners.com
Subject: [Histonet] HE stainers
To:
i need it too as we are going to bring new tissue processor to our small lab
--- On Sat, 6/26/10, Shirley Pan sj_...@yahoo.com wrote:
From: Shirley Pan sj_...@yahoo.com
Subject: [Histonet] Tissue Processors
To: histonet@lists.utsouthwestern.edu
Date: Saturday, June 26, 2010, 7:55 AM
We are in
dear histonetters
i have a quistion please regarding the thickness of lamina propria in small or
larg intestine.
what is the significant of it?? does it mean inflamation and pathological
condition or mean more size and so absorption of nutrients? i mean does the
thickning is favorable or not?
hi all histonetters
i need to do some morphomtric analysis on some samples of small intestin but we
have no image analysis software so i need to do it manually by occular
micrometer.
i need to know how to calculate villus surface area?
overall mucosal surface area of cross section?
surface
dear all
i have posted few days ago a quistion about enzyme significance in tissue??
eg. why i looking for alkaline phosphatase??? what it indicat??
i need a source or a sheet answering me
and i have nearly no response from you
any help her??
thanx
mohamed
dear histonetters
as i'm learning HC IHC i need to know a reference or internet site that could
help me to know the significance of different enzymes in tissues?? any help in
these!?
a second quistion please i'm trying to locat Alk. Phosphatase in chicken
intestine and i found in old reference
are you using bouin's , susa or formol zinker?? how many times do you use the
same fixtive? i know that zinker need to be freshly prepaired
thanxs
mohamed
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Dear histonetters
I wish to you, Happy Holidays with a lot of peace and health!
dr.Mohamed Abd el razik
Histology Dep.
Faculty of Vet. Med.
Cairo University- Egypt
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our cryostat is
Minotome Plus
Microtome Cryostat
Cat. No. 2563-- For 120 VAC, 60Hz
--- On Sat, 3/20/10, Cheryl Cornett-Early cornettear...@bellsouth.net wrote:
From: Cheryl Cornett-Early cornettear...@bellsouth.net
Subject: Re: [Histonet] cryostat help please!
To: mohamed abd el razik k8
i forget to introduce my self. i'm demonestrator of histology in faculty
of vet. med.
Cairo University- Egypt.(nearly 2 years experience) and i'm so happy to know
you all histoneters.
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hi all histoneters
i have learned alot from your posts and i need any suggestion about a cryostat
that was
working perfectly until the power cable is pluged off accidently. then after
about 2 days i put it again in the power and all is working with its motor
sound but no refregration and room
thanks for your replay ray
yes i set the temp. to -20 degrees but it is 20 for the last week.
--- On Sat, 3/20/10, Mark Ray darkd...@comcast.net wrote:
From: Mark Ray darkd...@comcast.net
Subject: Re: [Histonet] cryostat help please!
To: mohamed abd el razik k8...@yahoo.com
Date: Saturday
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