Immunostaining of Skeletal Tissues
- PMID: 32979208
- PMCID: PMC8365415
- DOI: 10.1007/978-1-0716-0989-7_15
Immunostaining of Skeletal Tissues
Abstract
Immunostaining is the process of identifying proteins in tissue sections by incubating the sample with antibodies specific to the protein of interest, then visualizing the bound antibody using a chromogen (immunohistochemistry or IHC) or fluorescence (immunofluorescence or IF). Unlike in situ hybridization, which identifies gene transcripts in cells, immunostaining identifies the products themselves and provides information about their localization within cells (nuclear, cytoplasmic, or membrane) or extracellular matrix. This can be particularly important in the context of bone and cartilage because they contain many cell types as well as matrix components, each with distinct protein expression patterns. As the number of antibodies continues to grow, this technique has become vital for research laboratories studying the skeleton. Here, we describe a detailed protocol for antibody-based in situ analysis of bone and associated tissues, addressing specific issues associated with staining of hard and matrix-rich tissues.
Keywords: Antibodies; Antigen retrieval; Bone; Cartilage; Decalcification; Fixation; Immunofluorescence; Immunohistochemistry; Immunostaining.
References
-
- Bord S (2003) Protein localization in wax-embedded and frozen sections of bone using immunohistochemistry. Methods Mol Med 80:237–247 - PubMed
-
- Freida CL, Hladik C. Histotechnology.; A self instructional text , 2009
-
- Sheehan DC, Hrapchak BB (1980) Theory and Practice of Histotechnology. 2nd ed. Bancroft JD, Stevens J, editors. St. Louis, MO, The CV Mosby Company
-
- L’Hoste RJ Jr, Tourres MA (1995) Using Zinc Formalin as a Routine Fixative in the Histology Laboratory. Lab Med 26(3):210–214
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous