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Upregulation of H2-M3 expression by exogenous N-formylated peptide. C57BL/6 splenocytes were cultured overnight in the absence (left panel) or presence (right panel) of N-Formyl-Met-Leu-Phe-Phe peptide (Sigma-Aldrich). The cells were then stained with either purified hamster anti- mouse H2-M3 mAb (clone 130) (open histograms) or purified hamster IgG1, κ isotype control mAb (clone A19-3) (Cat. No. 553969, filled histograms), in the presence of Mouse BD Fc Block™ purified anti-mouse CD16/CD32, mAb (clone 2.4G2) (Cat. No. 553141, open and filled histograms), followed by PE mouse anti-hamster IgG cocktail (Cat. No. 554056, open and filled histograms). Flow cytometry was performed on a BD FACSCalibur™ instrument.
BD Pharmingen™ Purified Hamster Anti-Mouse H2-M3
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Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
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- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Although hamster immunoglobulin isotypes have not been well defined, BD Biosciences Pharmingen has grouped Armenian and Syrian hamster IgG monoclonal antibodies according to their reactivity with a panel of mouse anti-hamster IgG mAbs. A table of the hamster IgG groups, Reactivity of Mouse Anti-Hamster Ig mAbs, may be viewed at http://www.bdbiosciences.com/documents/hamster_chart_11x17.pdf.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
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The hamster anti-mouse H2-M3 antibody (clone 130) reacts with the H2-M3 major histocompatibility complex (MHC) non-classical class Ib antigen. H2-M3 (M3) associates with β2-microglobulin and is capable of being expressed by most leukocytes. However, due to a lack of endogenous antigens, M3 has been reported to be undetectable on most cells. Its expression is induced by high-affinity N-formylated peptides from mitochondria, Listeria monocytogenes, and Mycobacterium tuberculosis. The induced expression of M3 is most efficient on antigen presenting cells. M3 presents antigen to cytotoxic T lymphocytes and may play a key role in protective immunity against the intracellular bacteria L. monocytogenes and M. tuberculosis. Furthermore, M3 is capable of presenting mitochondrial antigens for intrathymic positive selection of T-cell receptors which recognize those peptides.
Development References (6)
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Berg RE, Princiotta MF, Irion S, Moticka JA, Dahl KR, Staerz UD. Positive selection of an H2-M3 restricted T cell receptor. Immunity. 1999; 11(1):33-43. (Biology). View Reference
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Chiu NM, Chun T, Fay M, Mandal M, Wang CR. The majority of H2-M3 is retained intracellularly in a peptide-receptive state and traffics to the cell surface in the presence of N-formylated peptides. J Exp Med. 1999; 190(3):423-434. (Immunogen: Immunoprecipitation). View Reference
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Chun T, Serbina NV, Nolt D, et al. Induction of M3-restricted cytotoxic T lymphocyte responses by N-formylated peptides derived from Mycobacterium tuberculosis. J Exp Med. 2001; 193(10):1213-1220. (Biology). View Reference
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Lindahl KF, Byers DE, Dabhi VM, et al. H2-M3, a full-service class Ib histocompatibility antigen. Annu Rev Immunol. 1997; 15:851-879. (Biology). View Reference
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Seaman MS, Perarnau B, Lindahl KF, Lemonnier FA, Forman J. Response to Listeria monocytogenes in mice lacking MHC class Ia molecules. J Immunol. 1999; 162(9):5429-5436. (Biology). View Reference
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Shawar SM, Vyas JM, Rodgers JR, Rich RR. Antigen presentation by major histocompatibility complex class I-B molecules. Annu Rev Immunol. 1994; 12:839-880. (Biology). View Reference
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