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Tetramer: A structure composed of four identical smaller units, or four very similar smaller units. The units may be associated by covalent bonds or by noncovalent forces. This tetrapeptide is Gly-Gly-Gly-Gly, a tetramer composed of four identical amino acid residues (each is a glycine).
Tetramer analysis is a technique that uses MHC molecules to detect T-cells that recognize peptides or antigens from infected cells or cancerous cells. A tetramer has four MHC molecules attached to a streptavidin-coated bead. T-cells that recognize the peptide in the four MHC molecules will bind to the tetramer.
Tetramer stains usually analyze cytotoxic T lymphocyte (CTL) populations. CTLs are also called CD8+ T-cells, because they have CD8 co-receptors that bind to MHC class I molecules.
The tetramers used in the assay are made up of four major histocompatibility complex (MHC) molecules, which are found on the surface of most cells in the body.... Tetramer assaySynonymsTetramer stainPurposeuses tetrameric proteins to detect and quantify T cells
MHC tetramers are used for the analyses of T cell immunity, as these reagents allow accurate enumeration and efficient immunomagnetic sorting of antigen-specific T cells, regardless of the T cell's functional capacity.
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A tetramer assay (also known as a tetramer stain) is a procedure that uses tetrameric proteins to detect and quantify T cells that are specific for a given antigen within a blood sample.
In the presence of streptavidin which has four biotin binding sites per molecule, four MHC monomers are joined together to form a tetramer.
11.19. Major histocompatibility complex (MHC) tetramers are formed by first refolding MHCs in the presence of high concentrations of the desired antigenic peptide, followed by biotinylation of the carboxy-terminus of one chain of the MHC molecule.
In situ MHC-tetramer staining (IST) is a technique to visualize T cells that are specific for antigens of interest in tissues. In combination with immunohistochemistry (IHC), IST can determine the abundance, location, and phenotype of antigen-specific CD8 and CD4 T cells in tissues.
Generation of Tetramers: Transfer 30µl of peptide-exchanged monomer into a 1.5ml Eppendorf tube, or a new plate, then add 3.3µl of conjugated streptavidin, mix by pipetting up-and-down. Incubate on ice in the dark for 30 minutes. This is enough for about 15 tests.

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