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BD Pharmingen™ PE Mouse anti-Human CD160
クローン BY55 (RUO)

Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.

Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.



Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.

Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.

Flow cytometric analysis CD160 expression on human peripheral blood lymphocytes. Human whole blood cells were stained with APC Mouse Anti-Human CD56 (Cat. No. 555518) and either PE Mouse IgM, κ Isotype Control (Cat. No. 555584; Left Panel) or PE Mouse anti-Human CD160 (Cat. No. 562118; Right Panel). After incubation the erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-color dot plots showing the correlated expression of CD160 or background Ig isotype control staining versus CD56 were derived from gated events of the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.


ImageTitle~BD Pharmingen™ PE Mouse anti-Human CD160

ImageTitle~BD Pharmingen™ PE Mouse anti-Human CD160

Regulatory Statusの凡例
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
- 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).
- 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.
- Source of all serum proteins is from USDA inspected abattoirs located in the United States.
- An isotype control should be used at the same concentration as the antibody of interest.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
関連製品




The BY55 monoclonal antibody specifically binds to the human cell surface molecule, CD160 (also known as BY55). CD160 is a glycosyolphosphatidylinositol-anchored glycoprotein member of the immunoglobulin superfamily. It is expressed on cytotoxic αβ CD8+ T cells and natural killer (NK) cells, γδ T cells and intestinal intraepithelial T lymphocytes. CD160 can bind to classical and nonclassical MHC class I molecules. This interaction can costimulate the proliferation of activated human T lymphocytes including CD28-negative T lymphocytes.

Development References (3)
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Agrawal S, Marquet J, Freeman GJ, et al. Cutting edge: MHC class I triggering by a novel cell surface ligand costimulates proliferation of activated human T cells. J Immunol. 1999; 162(3):1223-1226. (Clone-specific: Flow cytometry). View Reference
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Anumanthan A, Bensussan A, Boumsell L, et al. Cloning of BY55, a novel Ig superfamily member expressed on NK cells, CTL, and intestinal intraepithelial lymphocytes. J Immunol. 1998; 161(6):2780-2790. (Clone-specific: Flow cytometry, Immunoprecipitation). View Reference
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Maiza H, Leca G, Mansur IG, Schiavon V, Boumsell L, Bensussan A. A novel 80-kD cell surface structure identifies human circulating lymphocytes with natural killer activity. J Exp Med. 1993; 178(3):1121-1126. (Clone-specific: Flow cytometry). 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.