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BD Pharmingen™ PE Mouse Anti-Mouse TCR Vδ6B
Clone F4.22.rMAb (also known as Anti-Vδ6λ12) (RUO)

Flow cytometric analysis of TCR Vδ6B expression on Mouse intraepithelial lymphocytes (IELs). C57BL/6 Mouse IELs were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141). The cells were then stained with BD OptiBuild™ R718 Hamster Anti-Mouse γδ T-Cell Receptor (Cat No. 751919), FITC Hamster Anti-Mouse CD3e (Cat. No. 553062) and with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; Left Plot) or PE Mouse Anti-Mouse TCR Vδ6B antibody (Cat. No. 570738/570739; Right Plot) at 0.5 μg/test. DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride) Solution (Cat. No. 564907) was added to cells right before analysis. The bivariate pseudocolor density plot showing the correlated expression of TCR Vδ6B (or Ig Isotype control staining) versus TCRγδ was derived from gated events with the forward and side light- scatter characteristics of viable (DAPI-negative) CD3-positive IELs. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.


Flow cytometric analysis of TCR Vδ6B expression on Mouse intraepithelial lymphocytes (IELs). C57BL/6 Mouse IELs were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141). The cells were then stained with BD OptiBuild™ R718 Hamster Anti-Mouse γδ T-Cell Receptor (Cat No. 751919), FITC Hamster Anti-Mouse CD3e (Cat. No. 553062) and with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; Left Plot) or PE Mouse Anti-Mouse TCR Vδ6B antibody (Cat. No. 570738/570739; Right Plot) at 0.5 μg/test. DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride) Solution (Cat. No. 564907) was added to cells right before analysis. The bivariate pseudocolor density plot showing the correlated expression of TCR Vδ6B (or Ig Isotype control staining) versus TCRγδ was derived from gated events with the forward and side light- scatter characteristics of viable (DAPI-negative) CD3-positive IELs. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.

Flow cytometric analysis of TCR Vδ6B expression on Mouse intraepithelial lymphocytes (IELs). C57BL/6 Mouse IELs were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141). The cells were then stained with BD OptiBuild™ R718 Hamster Anti-Mouse γδ T-Cell Receptor (Cat No. 751919), FITC Hamster Anti-Mouse CD3e (Cat. No. 553062) and with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; Left Plot) or PE Mouse Anti-Mouse TCR Vδ6B antibody (Cat. No. 570738/570739; Right Plot) at 0.5 μg/test. DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride) Solution (Cat. No. 564907) was added to cells right before analysis. The bivariate pseudocolor density plot showing the correlated expression of TCR Vδ6B (or Ig Isotype control staining) versus TCRγδ was derived from gated events with the forward and side light- scatter characteristics of viable (DAPI-negative) CD3-positive IELs. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.


BD Pharmingen™ PE Mouse Anti-Mouse TCR Vδ6B

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
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.
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- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- 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.
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- An isotype control should be used at the same concentration as the antibody of interest.
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- For U.S. patents that may apply, see bd.com/patents.
Companion Products






F4.22.RMAB is a recombinant form of the F4.22 monoclonal antibody. The F4.22 antibody specifically recognizes TCR Vδ6B subfamily members that have more than 90% identity at the nucleotide level with the previously described pλ12 and is also referred to as Anti-Vδ6λ12. The F4.22 antibody recognizes two members of the Vδ6/ADV subfamily expressed in C57BL/6 (B6) mice and at least one subfamily member expressed in DBA/2 mice. The F4.22 antibody does not recognize any TCR γδ T cell hybridomas expressing different TCR Vδ chains including other members of the TCR Vδ6 subfamily. The F4.22 antibody stains sizable proportions of Vγ1+, Vγ4+, and Vγ7+ γδ T cells prepared from the thymus, spleen, lymph nodes and intraepithelial lymphocytes (IELs) and T cell hybridomas derived from B6 mice. It likewise stains Vγ1+ and Vγ7+ γδ T cells from C57BL/10 and B10.D2 that share the same TCRδ haplotype. It does not stain any γδ T cells from BALB/c, C3H/HeJ, CBA/J, 129/Sv and FVB/N mice.

Development References (7)
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Azuara V, Grigoriadou K, Lembezat MP, Nagler-Anderson C, Pereira P. Strain-specific TCR repertoire selection of IL-4-producing Thy-1 dull gamma delta thymocytes. Eur J Immunol. 2001; 31(1):205-214. (Biology). View Reference
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Boucontet L, Grana M, Alzari PM, Pereira P. Mechanisms determining cell membrane expression of different gammadelta TCR chain pairings.. Eur J Immunol. 2009; 39(7):1937-46. (Biology). View Reference
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Chien YH, Iwashima M, Kaplan KB, Elliott JF, Davis MM. A new T-cell receptor gene located within the alpha locus and expressed early in T-cell differentiation.. Nature. 327(6124):677-82. (Biology). View Reference
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French JD, Roark CL, Born WK, O'Brien RL. Gammadelta T lymphocyte homeostasis is negatively regulated by beta2-microglobulin. J Immunol. 2009; 182(4):1892-1900. (Clone-specific: Flow cytometry). View Reference
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Pereira P, Berthault C, Burlen-Defranoux O, Boucontet L. Critical role of TCR specificity in the development of Vγ1Vδ6.3+ innate NKTγδ cells. J Immunol. 2013; 191(4):1716-1723. (Clone-specific: Flow cytometry). View Reference
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Pereira P, Hermitte V, Lembezat MP, Boucontet L, Azuara V, Grigoriadou K. Developmentally regulated and lineage-specific rearrangement of T cell receptor Valpha/delta gene segments.. Eur J Immunol. 2000; 30(7):1988-97. (Immunogen: Flow cytometry). View Reference
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Zeng W, O'Brien RL, Born WK, Huang Y. Characterization of Mouse γδ T Cell Subsets in the Setting of Type-2 Immunity.. Methods Mol Biol. 2018; 1799:135-151. (Clone-specific: Flow cytometry). View Reference
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
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.
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
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.