Immunohistochemistry or IHC refers to the process of localizing proteins in cells of a tissue section exploiting the principle of antibodies binding specifically to antigens in biological tissues. [1] It takes its name from the roots "immuno," in reference to antibodies used in the procedure, and "histo," meaning tissue (compare to immunocytochemistry). Immunohistochemical staining is widely used in the diagnosis of abnormal cells such as those found in cancerous tumors. Specific molecular markers are characteristic of particular cellular events such as proliferation or cell death (apoptosis). IHC is also widely used in basic research to understand the distribution and localization of biomarkers and differentially expressed proteins in different parts of a biological tissue.
Counterstaining is used in immunohistochemistry to provide contrast and enhance the visualization of specific cellular components. It involves applying a different colored dye to the sample, which binds to different structures than the primary antibody used to detect the target antigen. This helps to distinguish the specific cellular components of interest from the background, making them easier to identify and analyze under a microscope.
Some methods of biological investigations include microscopy, DNA sequencing, immunohistochemistry, and cell culture techniques. These methods allow researchers to study various aspects of living organisms, such as their structure, function, and interaction with the environment.
Xylene is an organic solvent which is miscible with alcohol and wax. In histochemistry alcohol is used to dehydrate tissue sections and then this alcohol is further replaced by xylene (being miscible with alcohol) in a process called as clearing. After this DPX is used to mount cover slips on the sections. One more use of xylene is to dissolve wax which is used to make sections of tissues. Hence, we see that xylene is a clearing agent capable of dissolving wax as well as alcohol.
Alternative methods to western blot for protein detection and analysis include enzyme-linked immunosorbent assay (ELISA), immunohistochemistry (IHC), mass spectrometry, and protein microarrays. These methods offer different advantages such as higher sensitivity, multiplexing capabilities, and the ability to analyze protein interactions.
1- What_is_the_different_staining_technique_in_virology2- What are the diffrent stain in micro for virus ?
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Immunohistochemistry information may be found in medical books, studies on biochemistry and physiological sciences. Medical schools have articles and resource materials which contain case studies in which immuunohistochemistry has been used to diagnose patients.
Paul Hirsch has written: 'Immunochemische Studien' -- subject(s): Immunohistochemistry
There could be multiple reasons why immunohistochemistry staining may work on control tissue but not on experimental tissue, such as differences in antigen expression, tissue processing methods, or antibody specificity. It's important to carefully review and troubleshoot the staining protocol, as well as consider factors like fixation and processing conditions that may affect the staining outcome. Additionally, confirming the presence of the antigen of interest in the experimental tissue using alternative methods can help identify potential issues with the immunohistochemistry staining.
Ethanol hydration in immunohistochemistry is used to rehydrate tissue sections that have been dehydrated during the staining process. This step allows for better penetration of antibodies and reagents into the tissue, improving the overall staining quality and specificity.
BioCare Medical provides high quality immunohistochemistry and molecular pathology products. They have ancillaries, antibodies, and equipment for detection.
Counterstaining is used in immunohistochemistry to provide contrast and enhance the visualization of specific cellular components. It involves applying a different colored dye to the sample, which binds to different structures than the primary antibody used to detect the target antigen. This helps to distinguish the specific cellular components of interest from the background, making them easier to identify and analyze under a microscope.
Mehrdad Nadji has written: 'Immunoperoxidase techniques' -- subject(s): Diagnosis, Handbooks, manuals, Immunoenzyme technics, Immunoenzyme technique, Immunohistochemistry, Neoplasms, Tumors
Some methods of biological investigations include microscopy, DNA sequencing, immunohistochemistry, and cell culture techniques. These methods allow researchers to study various aspects of living organisms, such as their structure, function, and interaction with the environment.
Hossein M. Yazdi has written: 'Diagnostic immunocytochemistry and electron microscopy' -- subject(s): Cancer, Cytodiagnosis, Diagnosis, Electron microscopic, Electron microscopy, Immunocytochemistry, Immunohistochemistry, Laboratory Diagnosis, Methods, Needle biopsy
Immunohistochemistry is a lab technique where a slide is made from a slice of tissue. It is treated with an antibody against the protein of interest that is made to bind to the protien with one end and and have a chemical reaction on the other. The chemical reaction can then be used to make the protein visible under the microscope.
Xylene is an organic solvent which is miscible with alcohol and wax. In histochemistry alcohol is used to dehydrate tissue sections and then this alcohol is further replaced by xylene (being miscible with alcohol) in a process called as clearing. After this DPX is used to mount cover slips on the sections. One more use of xylene is to dissolve wax which is used to make sections of tissues. Hence, we see that xylene is a clearing agent capable of dissolving wax as well as alcohol.