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Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Two-color flow cytometric analysis of Vγ1.1 TCR expression on mouse lymph node cells. C57BL/6 mouse lymph node cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142). The cells were then stained with either BD Horizon™ PE-CF594 Hamster Anti-Mouse γδ T-Cell Receptor antibody alone (Cat. No. 563532; Left Plot), or simultaneously with BD Horizon™ BV421 Vγ1.1 TCR antibody (Cat. No. 566308; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of γδ T-Cell Receptor versus Vγ1.1 TCR (or Autofluorescence), 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™ Flow Cytometer System.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
For optimal and reproducible results, BD Horizon Brilliant™ Stain Buffer should be used anytime BD Horizon Brilliant™ dyes are used in a multicolor flow cytometry panel. Fluorescent dye interactions may cause staining artifacts which may affect data interpretation. The BD Horizon Brilliant Stain Buffer was designed to minimize these interactions. When BD Horizon Brilliant Stain Buffer is used in in the multicolor panel, it should also be used in the corresponding compensation controls for all dyes to achieve the most accurate compensation. For the most accurate compensation, compensation controls created with either cells or beads should be exposed to BD Horizon Brilliant Stain Buffer for the same length of time as the corresponding multicolor panel. More information can be found in the Technical Data Sheet of the BD Horizon Brilliant Stain Buffer (Cat. No. 563794/566349) or the BD Horizon Brilliant Stain Buffer Plus (Cat. No. 566385).
The 2.11 monoclonal antibody recognizes the Vγ1.1 chain of the heterodimeric γδ T-cell receptor (TCR γδ) expressed by T lymphocytes and NK-T cells. It does not react with TCR αβ-bearing T cells. TCR γδ associates with CD3 molecules to form the TCR γδ/CD3 complex that mediates antigen recognition and can transduce intracellular signals leading to T cell responses. The Vγ1.1 TCR is also known as Vγ1 TCR. The Vγ1.1 variable region TCR gene segment primarily rearranges to join the Jγ4 and Cγ4 TCR gene segments. TCR Vγ1-expressing cells represent a major population of TCR γδ cells in the adult mouse thymus, peripheral lymphoid tissues, and different epithelia. They constitute a minor population of TCR γδ-positive T cells during fetal and early postnatal life.
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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.