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PE Mouse Anti-Human TCR Vβ13.2
PE Mouse Anti-Human TCR Vβ13.2
Two-color flow cytometric analysis of TCR Vβ13.2 expression on Human peripheral blood T lymphocytes. Human peripheral blood cells were stained with BD Horizon™ R718 Mouse Anti-Human CD3 (Cat. No. 566953) and with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; Left Plot) or PE Mouse Anti-Human TCR Vβ13.2 antibody (Cat. No. 568342/568343; Right Plot). Erythrocytes were lysed with BD FACS Lysing™ Solution (Cat. No. 349202). The bivariate pseudocolor density plot showing the correlated expression of TCR Vβ13.2 (or Ig Isotype control staining) versus CD3 was derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometry and data analysis were performed using BD FACSCelesta™ Cell Analyzer System and FlowJo™ software.
Two-color flow cytometric analysis of TCR Vβ13.2 expression on Human peripheral blood T lymphocytes. Human peripheral blood cells were stained with BD Horizon™ R718 Mouse Anti-Human CD3 (Cat. No. 566953) and with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; Left Plot) or PE Mouse Anti-Human TCR Vβ13.2 antibody (Cat. No. 568342/568343; Right Plot). Erythrocytes were lysed with BD FACS Lysing™ Solution (Cat. No. 349202). The bivariate pseudocolor density plot showing the correlated expression of TCR Vβ13.2 (or Ig Isotype control staining) versus CD3 was derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometry and data analysis were performed using BD FACSCelesta™ Cell Analyzer System and FlowJo™ software.
Product Details
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BD Pharmingen™
TCR V beta 13.2; TCR Vb13.2; TCRBV13S2; TCRBV6S2; TRBV6-2; TRBV62
Human (QC Testing)
Mouse SWR IgG1, κ
Human TCR Vβ13.2 Element Transfected Cell Line
Flow cytometry (Routinely Tested)
5 µl
Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide.
RUO


Preparation And Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to the dye under optimum conditions and unconjugated antibody and free dye were removed.

Recommended Assay Procedures

BD® CompBeads can be used as surrogates to assess fluorescence spillover (compensation).  When fluorochrome conjugated antibodies are bound to BD® CompBeads, they have spectral properties very similar to cells.   However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls.  It is strongly recommended that when using a reagent for the first time, users compare the spillover on cell and BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  3. 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.
  4. This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
  5. An isotype control should be used at the same concentration as the antibody of interest.
  6. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  7. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
568343 Rev. 2
Antibody Details
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H132

The H132 monoclonal antibody specifically recognizes the variable beta 13.2 region of the β subunit of the human αβ T cell receptor for antigen (TCR Vβ13.2). TCR Vβ13.2 is expressed on subsets of TCR αβ positive thymocytes and peripheral CD4+ and CD8+ T cells. The H132 antibody is useful for multiparameter analyses designed to study the nature of TCR Vβ13.2-positive cells including normal T cells as well as T cell clones, hybridomas, or tumors. It is also useful for analyzing TCR Vβ repertoires expressed by T cell populations collected from blood, tissues or other sources in health and disease models including inflammation, autoimmunity, responses to superantigens, tumors, and infectious diseases including HIV infection. The H132 antibody can reportedly stimulate the proliferation of TCR Vβ13.2-positive T cells. The H132 antibody recognizes human TCR Vβ13.2 subfamily members but does not react with other human TCR Vβ13 family members including TCR Vβ13.1, Vβ13.3, Vβ13.5 and Vβ13.6 subfamily members.

568343 Rev. 2
Format Details
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PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
altImg
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
568343 Rev.2
Citations & References
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View product citations for antibody "568343" on CiteAb

Development References (5)

  1. Choi YW, Kotzin B, Lafferty J, et al. A method for production of antibodies to human T-cell receptor beta-chain variable regions.. Proc Natl Acad Sci USA. 1991; 88(19):8357-61. (Immunogen: Flow cytometry, Functional assay, Stimulation). View Reference
  2. Dong T, Stewart-Jones G, Chen N, et al. HIV-specific cytotoxic T cells from long-term survivors select a unique T cell receptor.. J Exp Med. 2004; 200(12):1547-57. (Biology). View Reference
  3. Mongkolsapaya J, Jaye A, Callan MF, Magnusen AF, McMichael AJ, Whittle HC. Antigen-specific expansion of cytotoxic T lymphocytes in acute measles virus infection.. J Virol. 1999; 73(1):67-71. (Clone-specific: Flow cytometry). View Reference
  4. Moss P, Gillespie G, Frodsham P, Bell J, Reyburn H. Clonal populations of CD4+ and CD8+ T cells in patients with multiple myeloma and paraproteinemia.. Blood. 1996; 87(8):3297-306. (Clone-specific: Flow cytometry). View Reference
  5. Salameire D, Solly F, Fabre B, et al. Accurate detection of the tumor clone in peripheral T-cell lymphoma biopsies by flow cytometric analysis of TCR-Vβ repertoire.. Mod Pathol. 2012; 25(9):1246-57. (Clone-specific: Flow cytometry). View Reference
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568343 Rev. 2

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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.