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There is much more phosphotungstic acid in the solution than hematein. The phosphotungstic acid binds all of the available hematein to form a blue lake pigment. This lake stains the muscle cross striations, fibrin, nuclei, and other tissue elements blue. The rest of the phosphotungstic acid stains the red-brown components, such as collagen. [2]
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 .
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 .
Trichrome stains in which dyes and a polyacid are applied sequentially are called multi-step trichromes. In "one-step" methods, all the dyes—with or without a polyacid—are combined in a single solution. One of the oldest single-step approaches to trichrome staining is van Gieson's method, which stains muscle and cytoplasm yellow, and ...
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.
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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]
Depending on the formulation or staining technique, haematoxylin stains may be used in what is called a progressive manner, in which the length of time the tissue remains in contact with the staining solution is used to control the amount of colouration, or in a regressive manner, in which the tissue is over-stained, and excess stain is removed ...