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Flow cytometric analysis of Recombinant Human TIGIT Human IgG1 Fc Chimera Protein (TIGIT-Fc) binding blockade by Purified NA/LE Mouse Anti-Human TIGIT antibody on HeLa Cells. Cells from the human HeLa (Cervical adenocarcinoma, ATCC CCL-2) cell line were preincubated with either Recombinant Human IgG1 Fc Protein (Human IgG1 Fc; R&D Systems, Cat. No. 110-HG; 0.5 µg/test; Histogram 4) or Recombinant Human TIGIT Human IgG1 Fc Chimera Protein (TIGIT-Fc; R&D Systems Cat. No. 7898-TGB-100; 0.5 µg/test; Histogram 3). The binding of Recombinant Human TIGIT-Fc was blocked with Purified NA/LE Mouse Anti-Human TIGIT antibody (TgMab-2 Antibody; Cat. No. 568674; 20 µg/test; Histogram 2), but not blocked by Purified Mouse IgG1 κ Isotype Control (Isotype Control; Cat. No. 556648; 20 µg/test; Histogram 1). The degree of Human TIGIT-Fc binding was measured by fluorescent staining with Biotinylated Goat Anti-Human IgG (H+L) Antibody (Vector Lab, Cat. No. BA-3000-1.5) followed by PE Streptavidin (Cat. No. 554061). The histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
BD Pharmingen™ Purified NA/LE Mouse Anti-Human TIGIT
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Product Notices
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- An isotype control should be used at the same concentration as the antibody of interest.
- Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
Companion Products
The TgMab-2 monoclonal antibody specifically recognizes TIGIT (T cell Immunoreceptor with Ig and ITIM domains) which is also known as Vstm3 (V-set and transmembrane domain-containing 3), Vsig9 (V-set and Ig domain-containing 9) and WUCAM (Washington University Cell Adhesion Molecule). TIGIT is a 30-34 kDa single pass type I transmembrane glycoprotein that belongs to the CD28 family within the Ig superfamily. TIGIT has an extracellular region with a V-type Ig-like domain, transmembrane sequence, and a cytoplasmic domain with an immunoreceptor tyrosine-based inhibitory motif (ITIM). TIGIT is expressed on NK cells and subsets of activated and memory T cells, regulatory T cells (Treg), and T follicular helper (Tfh) cells. TIGIT binds to CD112 (PVRL2/Nectin-2) and CD155 (PVR/Necl-5) that are expressed on dendritic cells (DC), endothelial cells, fibroblasts, and some tumor cells and can induce IL-10 release and inhibition of IL-12 production. Ligand-bound TIGIT downregulates TCR-mediated T cell activation and proliferation and can block NK cell-mediated cytotoxicity.
Development References (3)
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Chiang EY, Mellman I. TIGIT-CD226-PVR axis: advancing immune checkpoint blockade for cancer immunotherapy.. J Immunother Cancer. 2022; 10(4):e004711. (Biology). View Reference
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Shibuya A, Shibuya K. DNAM-1 versus TIGIT: competitive roles in tumor immunity and inflammatory responses.. Int Immunol. 2021; 33(12):687-692. (Biology). View Reference
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Yu X, Harden K, Gonzalez LC, Francesco M, et al. The surface protein TIGIT suppresses T cell activation by promoting the generation of mature immunoregulatory dendritic cells. Nat Immunol. 2009; 10(1):48-57. (Biology). View Reference
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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.