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Purified NA/LE Mouse Anti-Human TIGIT
Purified NA/LE Mouse Anti-Human TIGIT

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.

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568674
¥97,020
EA (1 Each)
0.5 mg
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製品詳細
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BD Pharmingen™
T-cell immunoreceptor with Ig and ITIM domains; VSIG9; VSTM3; WUCAM
Human (QC Testing)
Mouse BALB/c IgG1, κ
Human TIGIT Transfected Cell Line
Blocking, Flow cytometry (Tested During Development)
1.0 mg/ml
AB_3684457
No azide/low endotoxin: Aqueous buffered solution containing no preservative, 0.2µm sterile filtered. Endotoxin level is ≤0.01 EU/µg (≤0.001 ng/µg) of protein as determined by the LAL assay.
RUO


Preparation and Storage

Store undiluted at 4°C. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. This preparation contains no preservatives, thus it should be handled under aseptic conditions.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  3. An isotype control should be used at the same concentration as the antibody of interest.
  4. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).

データシート

568674 Rev. 1
抗体の詳細
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TgMab-2

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.

568674 Rev. 1
フォーマットの詳細
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NA/LE
NA/LE refers to the culture and purification methods and buffer used to produce purified antibodies with no azide and low endotoxin: Aqueous buffered solution containing no preservative, 0.2µm sterile filtered. Endotoxin level is ≤0.01 EU/µg (≤0.001 ng/µg) of protein as determined by the LAL assay.NA/LE are perfectly suited to be used in culture or in vivo (for nonhuman studies) for functional assays — blocking, neutralizing, activation or depletion — where the presence of azide may damage cells or exogenous endotoxin may signal or activate cells.
NA/LE
568674 Rev.1
引用&参考文献
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Development References (3)

  1. 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
  2. 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
  3. 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
568674 Rev. 1

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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.