Trichrome Stain Kit (Connective Tissue Stain) ab150686 is intended for use in the histological visualization of collagenous connective tissue fibers in tissue sections.
Trichrome Stain Kit (Connective Tissue Stain) ab150686 is intended for use in the histological visualization of collagenous connective tissue fibers in tissue sections.
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Trichrome Stain Kit (Connective Tissue Stain) ab150686 is intended for use in the histological visualization of collagenous connective tissue fibers in tissue sections.
The trichrome stain kit may be used on formalin-fixed, paraffin-embedded. For frozen sections, it will require optimization by the user.
Trichrome stain protocol summary:
- deparaffinize sections if necessary
- preheat Bouin's Fluid to 54-64°C
- incubate slide in preheated Bouin's Fluid for 60 min and cool for 10 min
- rinse in water
- incubate slide in Weigert's Iron Hematoxylin for 5 min
- rinse in water
- incubate slide in Biebrich Scarlet / Acid Fuchsin solution for 15 min
- rinse in water
- differentiate in phosphomolybdic / phosphotungstic acid solution for 10-15 min
- incubate slide in Aniline Blue solution for 5-10 min
- rinse in water
- incubate slide in acetic acid solution for 3-5 min
- dehydrate, clear and mount
Other products for staining tissue sections
Find more kits and reagents in the special stains guide, or products for antigen retrieval, blocking, signal amplification, visualization, counterstaining, and mounting in the IHC kits and reagents guide.
Staining Interpretation
Collagen | Blue |
Muscle Fibers | Red |
Nuclei | Dark Red to Black/Blue |
Control Tissue: Lung, Uterus, Small Intestine, Stomach.
Collagenous connective tissue fibers often referred to simply as collagen fibers are essential structural components in various tissues including skin bone tendons and ligaments. These fibers with a molecular mass that can vary depending on the type of collagen provide tensile strength and support to tissues and organs. They are synthesized by fibroblasts and expressed abundantly in extracellular matrix environments. Collagenous fibers are identifiable using Masson's trichrome staining which helps differentiate these fibers in histological studies.
Collagenous fibers contribute to the mechanical framework of connective tissues enabling them to resist stretching and deformation. They are part of larger complexes that include elastin and proteoglycans working together to maintain tissue integrity and function. These fibers interact with other cellular components through specific receptors like integrins which mediate signals for cellular processes including differentiation adhesion and migration.
Collagenous connective tissue fibers play roles in wound healing and tissue remodeling. They participate in pathways involving matrix metalloproteinases (MMPs) which regulate the degradation of extracellular matrix components. The collagen synthesis and cross-linking process often links with proteins such as fibronectin and laminin which influence cell behavior and tissue repair mechanisms.
Defective or insufficient collagenous connective tissue fibers can lead to conditions like Ehlers-Danlos syndrome and osteogenesis imperfecta. Both disorders reflect abnormalities in collagen synthesis or structure resulting in increased tissue fragility and elasticity issues. Mutations in collagen-related genes often underlie these pathologies highlighting the importance of these fibers in maintaining structural and functional integrity of various tissues.
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ab150686 Trichrome Stain Kit (Connective Tissue Stain) staining formalin-fixed-paraffin embedded human muscle.
ab150686 (Trichrome Stain) staining collagen (blue) and muscle fibre (red) in formalin fixed paraffin embedded normal human placenta. Nuclei are counterstained with Weigert's hematoxylin (blue)
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.
A paraffin-embedded section of healthy mouse spleen stained with ab150686 - Trichrome Stain Kit (Connective Tissue Stain). The sample was deparaffinized by heating to 60°C for 1 hour and then deparaffinization following a standard protocol. Sections were then fixed with Bouin's solution (included in the kit) for 1 hour at 60°C in humid conditions.
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