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BD Pharmingen™ PE-Cy™7 Hamster Anti-Mouse TCR β Chain
Clone H57-597 (RUO)

Flow cytometric analysis of the T-cell receptor (TcR) β-chain on mouse splenocytes. Left Panel: Splenocytes from BALB/c mice were either unstained (shaded) or stained with the PE-Cy™7 Hamster Anti-Mouse TcR β-chain antibody (unshaded). Middle and Right Panels: Splenocytes from BALB/c mice were stained with both a FITC Rat Anti-Mouse CD4 antibody (Cat.No. 553047) and a FITC Rat Anti-Mouse CD8a antibody (Cat.No. 553031) in conjunction with either no other staining (autofluorescence) (middle panel) or with the PE-Cy7 Hamster Anti-Mouse TcR β-chain antibody (right panel). Histograms and dot plots were derived from gated events based on light scattering characteristics for splenocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.

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Flow cytometric analysis of the T-cell receptor (TcR) β-chain on mouse splenocytes. Left Panel: Splenocytes from BALB/c mice were either unstained (shaded) or stained with the PE-Cy™7 Hamster Anti-Mouse TcR β-chain antibody (unshaded). Middle and Right Panels: Splenocytes from BALB/c mice were stained with both a FITC Rat Anti-Mouse CD4 antibody (Cat.No. 553047) and a FITC Rat Anti-Mouse CD8a antibody (Cat.No. 553031) in conjunction with either no other staining (autofluorescence) (middle panel) or with the PE-Cy7 Hamster Anti-Mouse TcR β-chain antibody (right panel). Histograms and dot plots were derived from gated events based on light scattering characteristics for splenocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.

Flow cytometric analysis of the T-cell receptor (TcR) β-chain on mouse splenocytes. Left Panel: Splenocytes from BALB/c mice were either unstained (shaded) or stained with the PE-Cy™7 Hamster Anti-Mouse TcR β-chain antibody (unshaded). Middle and Right Panels: Splenocytes from BALB/c mice were stained with both a FITC Rat Anti-Mouse CD4 antibody (Cat.No. 553047) and a FITC Rat Anti-Mouse CD8a antibody (Cat.No. 553031) in conjunction with either no other staining (autofluorescence) (middle panel) or with the PE-Cy7 Hamster Anti-Mouse TcR β-chain antibody (right panel). Histograms and dot plots were derived from gated events based on light scattering characteristics for splenocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
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BD Pharmingen™ PE-Cy™7 Hamster Anti-Mouse TCR β Chain
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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
- 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.
- Warning: Some APC-Cy7 and PE-Cy7 conjugates show changes in their emission spectrum with prolonged exposure to formaldehyde. If you are unable to analyze fixed samples within four hours, we recommend that you use BD™ Stabilizing Fixative (Cat. No. 338036).
- Please observe the following precautions: Absorption of visible light can significantly alter the energy transfer occurring in any tandem fluorochrome conjugate; therefore, we recommend that special precautions be taken (such as wrapping vials, tubes, or racks in aluminum foil) to prevent exposure of conjugated reagents, including cells stained with those reagents, to room illumination.
- Cy is a trademark of GE Healthcare.
- PE-Cy7 is a tandem fluorochrome composed of R-phycoerythrin (PE), which is excited by 488-nm light and serves as an energy donor, coupled to the cyanine dye Cy7, which acts as an energy acceptor and fluoresces maximally at 780 nm. PE-Cy7 tandem fluorochrome emission is collected in a detector for fluorescence wavelengths of 750 nm and higher. Although every effort is made to minimize the lot-to-lot variation in the efficiency of the fluorochrome energy transfer, differences in the residual emission from PE may be observed. Therefore, we recommend that individual compensation controls be performed for every PE-Cy7 conjugate. PE-Cy7 is optimized for use with a single argon ion laser emitting 488-nm light, and there is no significant overlap between PE-Cy7 and FITC emission spectra. When using dual-laser cytometers, which may directly excite both PE and Cy7, we recommend the use of cross-beam compensation during data acquisition or software compensation during data analysis.
- 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.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
Companion Products

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The H57-597 antibody reacts with a common epitope of the β chain of the T-cell Receptor (TCR) complex on αβ TCR-expressing thymocytes, peripheral T lymphocytes, NK1.1+ thymocytes, and NK-T cells of all mouse strains tested. It does not react with γδ TCR-bearing T cells. In the fetal and adult thymus, the TCR β-chain may form homodimers or pair with the pre-TCR α-chain on the surface of immature thymocytes before TCR α-chain expression. Plate-bound or soluble H57-597 antibody activates αβ TCR-bearing T cells, and plate-bound mAb can induce apoptotic death.

Development References (3)
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Gascoigne NR. Transport and secretion of truncated T cell receptor beta-chain occurs in the absence of association with CD3. J Biol Chem. 1990; 265(16):9296-9301. (Clone-specific: Immunofluorescence, Immunoprecipitation). View Reference
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Kruisbeek AM, Shevach EM. Proliferative assays for T cell function. Curr Protoc Immunol. 2004; 3:3.12.1-3.12.14. (Clone-specific: Activation, Functional assay, Stimulation). View Reference
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Kubo RT, Born W, Kappler JW, Marrack P, Pigeon M. Characterization of a monoclonal antibody which detects all murine alpha beta T cell receptors. J Immunol. 1989; 142(8):2736-2742. (Immunogen: Activation, Flow cytometry, Functional assay, Stimulation). View Reference
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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.