Mouse Immune Cell Phenotyping IHC Antibody Sampler Kit #37495
Product Information
Kit Usage Information
Protocols
- 12653: Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Immunofluorescence, Flow*
- 25229: Western Blotting, Immunohistochemistry (LEICA® BOND™), Immunohistochemistry (Paraffin)
- 44153: Western Blotting, Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Flow
- 70076: Western Blotting, Immunoprecipitation (Agarose), Immunohistochemistry (Paraffin)
- 78588: Western Blotting, Immunoprecipitation (Magnetic), Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Immunofluorescence
- 90176: Western Blotting, Immunoprecipitation (Agarose), Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Flow
- 97585: Western Blotting, Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence
- 98941: Western Blotting, Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin)
Product Description
The Mouse Immune Cell Phenotyping IHC Antibody Sampler Kit provides an economical means of detecting the accumulation of immune cell types in formalin-fixed, paraffin-embedded tissue samples.
Background
Cluster of Differentiation 3 (CD3) is a multiunit protein complex expressed on the surface of T-cells that directly associates with the T-cell receptor (TCR). CD3 is composed of four polypeptides: ζ, γ, ε and δ. Engagement of TCR complex with antigens presented in Major Histocompatibility Complexes (MHC) induces tyrosine phosphorylation in the immunoreceptor tyrosine-based activation motif (ITAM) of CD3 proteins. CD3 phosphorylation is required for downstream signaling through ZAP-70 and p85 subunit of PI-3 kinase, leading to T cell activation, proliferation, and effector functions (1). Cluster of Differentiation 8 (CD8) is a transmembrane glycoprotein expressed primarily on cytotoxic T cells, but has also been described on a subset of dendritic cells in mice (2,3). On T cells, CD8 is a co-receptor for the TCR, and these two distinct structures are required to recognize antigen bound to MHC Class I (2). Cluster of Differentiation 4 (CD4) is expressed on the surface of T helper cells, regulatory T cells, monocytes, macrophages, and dendritic cells, and plays an important role in the development and activation of T cells. On T cells, CD4 is the co-receptor for the TCR, and these two distinct structures recognize antigen bound to MHC Class II. CD8 and CD4 co-receptors ensure specificity of the TCR–antigen interaction, prolong the contact between the T cell and the antigen presenting cell, and recruit the tyrosine kinase Lck, which is essential for T cell activation (2). Granzyme B is a serine protease expressed by CD8+ cytotoxic T lymphocytes and natural killer (NK) cells and is a key component of the immune response to pathogens and transformed cancer cells (4). Forkhead box P3 (FoxP3) is crucial for the development of T cells with immunosuppressive regulatory properties and is a well-established marker for T regulatory cells (Tregs) (5). CD19 is a co-receptor expressed on B cells that amplifies the signaling cascade initiated by the B cell receptor (BCR) to induce activation. It is a biomarker of B lymphocyte development, lymphoma diagnosis, and can be utilized as a target for leukemia immunotherapies (6,7). F4/80 (EMR1) is a heavily glycosylated G-protein-coupled receptor and is a well-established marker for mouse macrophages (8). CD11c (integrin αX, ITGAX) is a transmembrane glycoprotein highly expressed by dendritic cells, and has also been observed on activated NK cells, subsets of B and T cells, monocytes, granulocytes, and some B cell malignancies including hairy cell leukemia (9,10).
- Kuhns, M.S. et al. (2006) Immunity 24, 133-9.
- Zamoyska, R. (1994) Immunity 1, 243-6.
- Shortman, K. and Heath, W.R. (2010) Immunol Rev 234, 18-31.
- Trapani, J.A. (2001) Genome Biol 2, REVIEWS3014.
- Ochs, H.D. et al. (2007) Immunol Res 38, 112-21.
- Tedder, T.F. et al. (1997) Immunity 6, 107-18.
- Scheuermann, R.H. and Racila, E. (1995) Leuk Lymphoma 18, 385-97.
- McKnight, A.J. et al. (1996) J Biol Chem 271, 486-9.
- Kohrgruber, N. et al. (1999) J Immunol 163, 3250-9.
- Qualai, J. et al. (2016) PLoS One 11, e0154253.
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