HSP Antibodies
Heat Shock Protein (HSP) antibodies target members of the heat shock protein family, which are molecular chaperones crucial for maintaining cellular proteostasis. HSPs help in the proper folding, assembly, and degradation of proteins, especially under stress conditions such as heat shock, oxidative stress, and inflammation.
Content of HSP Antibody
HSP antibodies are developed to specifically bind to members of the HSP family. These antibodies are generated using synthetic peptides or recombinant proteins representing conserved or unique regions of specific HSP isoforms. Immunogen: Synthetic peptides or recombinant proteins from specific HSP family members (e.g., HSP27, HSP70, HSP90).
- Host: Typically raised in rabbits or mice.
- Applications: Suitable for Western blotting (WB), immunoprecipitation (IP), immunohistochemistry (IHC), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA).
- Reactivity: Commonly reactive with human, mouse, and rat HSP proteins, with potential cross-reactivity in other species depending on the isoform.
Application of HSP Antibody
HSP antibodies are widely used in research fields related to stress response, cell survival, cancer biology, and neurodegenerative diseases. The applications include:
- Western Blotting (WB): HSP antibodies are applied to detect and quantify the expression levels of HSP proteins in cell or tissue lysates. This is important for analyzing how cells respond to stress conditions and for studying alterations in HSP expression during disease development, particularly in cancer and neurodegeneration.
- Immunohistochemistry (IHC): HSP antibodies enable the visualization of HSP expression in tissue sections, allowing researchers to examine the localization of these chaperone proteins in different tissues or under various stress conditions. IHC is particularly useful in studying tumors or damaged tissues where HSP expression is elevated.
- Immunoprecipitation (IP): HSP antibodies are used to isolate HSP proteins from cell lysates for studying protein-protein interactions. This helps in understanding how HSPs form complexes with other proteins to facilitate their folding, stability, or degradation, especially under stress.
HSP antibodies are key tools in understanding the mechanisms underlying cellular protection against stress, the regulation of protein quality control, and the role of HSPs in diseases like cancer, Alzheimer’s, Parkinson’s, and other conditions associated with protein misfolding and aggregation.
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