Great folks in histonet,
Can any of you have done or having experience in IHC detection of LAMP-2 and
Adipophilin on formalin fixed paraffin sections of mouse. I am working on
differentiating phospholipidosis and neutral lipidosis in mouse tissues. please
share your experience/protocol.
All,
I would like to quantify collagen 1 in bleomycin induced lung fibrosis in mice.
It will be highly appreciated if any of our histonetters will share their
protocol for IHC staining of perfusion fixed(10% NBF) mouse fibrotic lungs.
Thanks in advance
Abi
Dear Histonetters,
I am looking for hearing from our experienced histonetters regarding the
possibility of staining of immature collagen fibres in animal models of lung
fibrosis. I didn't find any histochemical method in the literature to stain the
immature collagen. I would like to know
Dear Fello histonetters,
I am looking for demonstration of demyelination in rat spinal cord paraffin
sections. A quick look into the literature revealed use of combination of luxol
fast blue and PAS for demonstration of demyelination and myelin breakdown
products. Anybody over here will
Dear Histonetters,
I am requesting your valuable advice/suggestion on immunohistochemical staining
of macrophages in rat mesentery adipose tissue. I would like to know the type
of primary and secondary antibodies you are using(manufacturer details)and your
preferable protocol etc.
Thanks
Dear fellow histonetters,
I would like to know from your experience with respect to collection, trimming
and embedding of mesentery from rat. Our pathologists are interested in light
microscopic examination of blood vessels of mesentery from rat. The objective
is to get as many as blood
Dear fellow histonetters,
I would like to have your suggestions regarding trimming and sectioning of
mouse heart. Our pathologists are interested in evaluating mouse ventricle
papillary muscle for some lesions. I am not able to cut sections having
papillary muscle in all sections.Some
Hello
I need your advice regarding paraffin sections of rat kidney. Kidneys are
collected, adequately fixed with 10 % NBF and undergone routine tissue
processing in Sakura VIP 6 tissue processor.Sections are of 5 micron thickness.
Strangely, in the HE stained sections, our pathologists are
Dear Histonetters,
Our pathologists are interested in rat heart valvular lesions. I am working on
trimming and sectioning methods to get uniform and reproducible morphology of
heart valves in paraffin sections. It seems that available literature dealing
with this is limited. Requesting your
Dear Histonetters,
We were asked to process Hamster tissue(Large intestine) for one of our
investigators. I would like to know whether any of our users process hamster
tissues in their labs, if so kindly provide me a protocol for the same. Our
tissue processor is Sakura VIP6.
Thanks for all
Dear Histonetters,
We would like to procure one tissue auto stainer for our histology lab(mainly
HE staining) In this respect, I request your experience about Microm HMS 740
automatic stainer. Please share your comments regarding the staining
reproducibility,ease of handling and their claim
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