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It is used to show gliosis in the central nervous system, tumours of skeletal muscles, and fibrin deposits in lesions. Muscle is stained blue-black to dark brown, connective tissue is pale orange-pink to brownish red, fibrin and neuroglia stain deep blue, coarse elastic fibers show as purple, and bone and cartilage obtain yellowish to brownish ...
Dilated peri-tubular capillaries filled with sickled RBCs, original Gomori's trichrome stain, × 400. [1] The "ragged red fibers" in MELAS syndrome are visible under modified Gomori stain. Gömöri trichrome stain is a histological stain used on muscle tissue. [2] [3] It can be used to test for certain forms of mitochondrial myopathy.
Mouse skin stained with Masson's trichrome stain. Masson's trichrome is a three-colour staining procedure used in histology . The recipes emerged from Claude L. Pierre Masson 's (1880–1959) original formulation have different specific applications, but all are suited for distinguishing cells from surrounding connective tissue .
Van Gieson's stain is a mixture of picric acid and acid fuchsin. It is the simplest method of differential staining of collagen and other connective tissue . It was introduced to histology by American neuropsychiatrist and pathologist Ira Van Gieson .
Hematoxylin and eosin stain. Soft tissue connects and surrounds or supports internal organs and bones, and includes muscle, tendons, ligaments, fat, fibrous tissue, lymph and blood vessels, fasciae, and synovial membranes. [1] [2] Soft tissue is tissue in the body that is not hardened by the processes of ossification or calcification such as ...
Masson's trichrome staining on rat trachea. Hematoxylin and eosin is one of the most commonly used stains in histology to show the general structure of the tissue. [9] [19] Hematoxylin stains cell nuclei blue; eosin, an acidic dye, stains the cytoplasm and other tissues in different stains of pink. [9] [12]
Lawsone reacts chemically with the protein keratin in skin and hair via a Michael addition reaction, resulting in a strong permanent stain that lasts until the skin or hair is shed. Darker colored staining is due to more lawsone–keratin interactions occurring, which evidently break down as the concentration of lawsone decreases and the tattoo ...
Luxol fast blue stain, abbreviated LFB stain or simply LFB, is a commonly used stain to observe myelin under light microscopy, created by Heinrich Klüver and Elizabeth Barrera in 1953. [1] LFB is commonly used to detect demyelination in the central nervous system (CNS), but cannot discern myelination in the peripheral nervous system .