HE -
stained brain section showing focal gliosis (arrow)(D).
Mock - infected control (A); Severe hemorrhage and regression of ovarian follicles (B); Spleens from mock - infected control (left) and enlarged spleens from the infected ducks (C); HE - stained ovary section showing hemorrhage and follicle rupture with red stained bodies (D); HE -
stained brain section revealing lymphocytes and mononuclear cell infiltration under cranial arachnoid (E) and focal gliosis (arrow)(F).
The Stain This brain section, from another donor, is in the midst of receiving a silver - based stain that darkens myelin, revealing the fibers that connect brain regions.
Not exact matches
Part of the tissue from the formaldehyde
sections is
stained, pressed into slides, and put under the microscope to verify the
brain's condition, healthy or diseased.
The antibodies used for this slide are from left to right, ab92547, this is a rabbit monoclonal antibody to vimentin and in this image it is
staining astrocytes in Macaque
brain sections.
To further validate our inclusion / exclusion co-localization analysis we then
stained rat
brain sections with MAOB - 2, a monoclonal antibody directed to residues 1 — 4 of Aβ, and which has been reported as absent of cross-reactivity with APP or CTFs [39].
and affinity of antibody ACI - 5400 were characterized by a panel of methods: (i) measuring the selectivity for a specific phospho - Tau epitope known to be associated with tauopathy, (ii) performing a combination of peptide and protein binding assays, (iii)
staining of
brain sections from mouse preclinical tauopathy models and from human subjects representing six different tauopathies, and (iv) evaluating the selective binding to pathological epitopes on extracts from tauopathy
brains in non-denaturing sandwich assays.
ab7260
staining rat
brain tissue
sections by IHC - P.
IHC image of GFAP
staining in a formalin fixed, paraffin embedded normal rat
brain tissue
section, performed on a Leica Bond ™ system using the standard protocol F.