Customer Service: (855) 848-6626 | 8:00 a.m - 4:30 p.m. PST | Receive a Free Mask with Orders over $300

C57Bl/6 splenocytes were stained with 0.5 ug violetFluor™ 450 Anti-Mouse CD3 (75-0032) (solid line) or 0.5 ug violetFluor™ 450 Rat IgG2b isotype control (dashed line).
  • C57Bl/6 splenocytes were stained with 0.5 ug violetFluor™ 450 Anti-Mouse CD3 (75-0032) (solid line) or 0.5 ug violetFluor™ 450 Rat IgG2b isotype control (dashed line).
  • violetFluor™ 450 Anti-Mouse CD3 (17A2)

violetFluor™ 450 Anti-Mouse CD3 (17A2)

Cat No. Size Price Quantity
75-0032-U025 25 µg $51.00
75-0032-U100 100 µg $115.00

Description

The 17A2 antibody reacts with the mouse CD3 complex, comprised of CD3 epsilon, CD3 gamma and CD3 delta. These integral membrane protein chains assemble with additional chains of the T cell receptor (TCR), as well as CD3 zeta chain, to form the T cell receptor – CD3 complex. Together with co-receptors CD4 or CD8, the complex serves to recognize antigens bound to MHC molecules on antigen-presenting cells. Such interactions promote T cell receptor signaling (T cell activation) and can result in a number of cellular responses including proliferation, differentiation, production of cytokines or activation-induced cell death. CD3 is differentially expressed during thymocyte-to-T cell development and on all mature T cells.

The 17A2 antibody is a widely used phenotypic marker for mouse T cells. In addition, as the CD3e chain within the TCR complex contains intracellular signaling domains, binding of 17A2 antibody to CD3 can induce cell activation (use format suitable for functional assays). A recent publication of the crystal structure of a murine CD3e-mitogenic antibody complex provides further insight into the action of commonly used agonist antibodies (Fernandes, R.A. et al. 2012. Journal of Biological Chemistry. 287: 13324-13335).

Recent Publications:

Andersen TK, Huszthy PC, Gopalakrishnan RP, et al. Enhanced germinal center reaction by targeting vaccine antigen to major histocompatibility complex class II molecules. NPJ Vaccines. 2019;4:9. Published 2019 Feb 11. doi:10.1038/s41541-019-0101-0.

» View on PubMed

Perez J, Dansou B, Herve R, Levi C, Tamouza H, Vandermeersch S, Demey-Thomas E, Haymann JP, Zafrani L, Klatzmann D, Boissier MC, Letavernier E and Baud L. 2015. J Immunol. doi: 10.4049/jimmunol.1500749. (Flow Cytometry)

View More

The 17A2 antibody reacts with the mouse CD3 complex, comprised of CD3 epsilon, CD3 gamma and CD3 delta. These integral membrane protein chains assemble with additional chains of the T cell receptor (TCR), as well as CD3 zeta chain, to form the T cell receptor – CD3 complex. Together with co-receptors CD4 or CD8, the complex serves to recognize antigens bound to MHC molecules on antigen-presenting cells. Such interactions promote T cell receptor signaling (T cell activation) and can result in a number of cellular responses including proliferation, differentiation, production of cytokines or activation-induced cell death. CD3 is differentially expressed during thymocyte-to-T cell development and on all mature T cells.

The 17A2 antibody is a widely used phenotypic marker for mouse T cells. In addition, as the CD3e chain within the TCR complex contains intracellular signaling domains, binding of 17A2 antibody to CD3 can induce cell activation (use format suitable for functional assays). A recent publication of the crystal structure of a murine CD3e-mitogenic antibody complex provides further insight into the action of commonly used agonist antibodies (Fernandes, R.A. et al. 2012. Journal of Biological Chemistry. 287: 13324-13335).

Recent Publications:

Andersen TK, Huszthy PC, Gopalakrishnan RP, et al. Enhanced germinal center reaction by targeting vaccine antigen to major histocompatibility complex class II molecules. NPJ Vaccines. 2019;4:9. Published 2019 Feb 11. doi:10.1038/s41541-019-0101-0.

» View on PubMed

Perez J, Dansou B, Herve R, Levi C, Tamouza H, Vandermeersch S, Demey-Thomas E, Haymann JP, Zafrani L, Klatzmann D, Boissier MC, Letavernier E and Baud L. 2015. J Immunol. doi: 10.4049/jimmunol.1500749. (Flow Cytometry)

Hide

Product Details

Name violetFluor™ 450 Anti-Mouse CD3 (17A2)
Cat. No. 75-0032
Alternative Names CD3 epsilon
Gene ID 12502
Clone 17A2
Isotype Rat IgG2b, κ
Reactivity Mouse
Cross Reactivity
Format violetFluor™ 450
Application Flow Cytometry
Citations*

Andersen TK, Huszthy PC, Gopalakrishnan RP, et al. Enhanced germinal center reaction by targeting vaccine antigen to major histocompatibility complex class II molecules. NPJ Vaccines. 2019;4:9. Published 2019 Feb 11. doi:10.1038/s41541-019-0101-0.

» View on PubMed

Joetham A, Ohnishi H, Okamoto M, Takeda K, Schedel M, Domenico J, Dakhama A, and Gelfand EW. 2012. J. Biol. Chem. 287:17100-17108. (in vitro activation)

Kasahara S and Clark, EA. 2012. J. Leukoc. Biol. 91:437-448. (in vitro activation)

Xiao J, Julianty A, Wen J, Smith SV, Park PW, Ford ML, Haller CA, and Chaikof EL. 2012. Arterioscler. Thromb. Vasc. Biol. 32:386-396. (in vivo T cell depletion)

Miescher GC, Schreyer M, and MacDonald HR. 1989. Immunol. Lett. 23: 113-118. (Origination of clone 17A2, Functional Assay, Immunohistochemistry, Immunoprecipitation)

Application Key:

FC = Flow Cytometry; FA = Functional Assays; ELISA = Enzyme-Linked Immunosorbent Assay; ICC = Immunocytochemistry; IF = Immunofluorescence Microscopy; IHC = Immunohistochemistry; IHC-F = Immunohistochemistry, Frozen Tissue; IHC-P = Immunohistochemistry, Paraffin-Embedded Tissue; IP = Immunoprecipitation; WB = Western Blot; EM = Electron Microscopy

*Tonbo Biosciences tests all antibodies by flow cytometry. Citations are provided as a resource for additional applications that have not been validated by Tonbo Biosciences. Please choose the appropriate format for each application and consult the Materials and Methods section for additional details about the use of any product in these publications.