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Two-color flow cytometric analysis of mouse CD161b expression on C57BL/6 mouse splenocytes. Mouse splenic leucocytes were stained with BV421 Mouse Anti-Mouse NK1.1 antibody (Cat. No. 562921) and either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (Cat. No. 557690; Left Plot) or Alexa Fluor® 647 Rat Anti-Mouse CD161a antibody (Cat. No. 566307; Right Plot). Two-color flow cytometric contour plots showing the correlated expression of NK1.1 versus CD161b (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. Flow cytometric analysis was performed using a BD FACSCanto™ II Flow Cytometer System.
BD Pharmingen™ Alexa Fluor® 647 Rat Anti-Mouse CD161b
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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.
- 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.
- The Alexa Fluor®, Pacific Blue™, and Cascade Blue® dye antibody conjugates in this product are sold under license from Molecular Probes, Inc. for research use only, excluding use in combination with microarrays, or as analyte specific reagents. The Alexa Fluor® dyes (except for Alexa Fluor® 430), Pacific Blue™ dye, and Cascade Blue® dye are covered by pending and issued patents.
- Alexa Fluor® 647 fluorochrome emission is collected at the same instrument settings as for allophycocyanin (APC).
- Alexa Fluor® is a registered trademark of Molecular Probes, Inc., Eugene, OR.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
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Companion Products
The 2D9 monoclonal antibody recognizes C57BL/6 mouse Natural killer cell receptor P1D (NKR-P1D) which is also known as NKR-P1B[B6], or CD161b. CD161b is encoded by Klrb1b (killer cell lectin-like receptor subfamily B member 1B). CD161b is expressed by a functionally distinct subset of natural killer (NK) cells that express higher levels of cytotoxicity and interferon-γ (IFN-γ) than their CD161b-low or -negative counterparts. CD161b is a type II transmembrane glycoprotein that contains an immunoreceptor tyrosine-based inhibitory motif in its cytoplasmic domain. CD161b binds to C-type lectin related protein b (Clr-b) and may play a role in regulating NK cell responses. The 2D9 antibody has slight crossreactivity with cells transfected with Klrb1a/NKRP1A, Klrb1c/NKRP1C, or Klrb1f/NKRP1F.
Development References (6)
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Aust JG1, Gays F, Mickiewicz KM, Buchanan E, Brooks CG.. The expression and function of the NKRP1 receptor family in C57BL/6 mice.. J Immunol. 2009; 183(1):106-116. (Immunogen: Blocking, Flow cytometry, Fluorescence activated cell sorting). View Reference
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Giorda R, Trucco M. Mouse NKR-P1. A family of genes selectively coexpressed in adherent lymphokine-activated killer cells. J Immunol. 1991; 147(5):1701-1708. (Biology). View Reference
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Kirkham CL, Carlyle JR. Complexity and Diversity of the NKR-P1:Clr (Klrb1:Clec2) Recognition Systems. Front Biosci. 2014; 5(5):1-16. (Biology). View Reference
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Kung SK, Su RC, Shannon J, Miller RG. The NKR-P1B gene product is an inhibitory receptor on SJL/J NK cells. J Immunol. 1999; 162(10):5876-5887. (Biology). View Reference
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Plougastel B, Matsumoto K, Dubbelde C, Yokoyama WM. Analysis of a 1-Mb BAC contig overlapping the mouse Nkrp1 cluster of genes: cloning of three new Nkrp1 members, Nkrp1d, Nkrp1e, and Nkrp1f.. Immunogenetics. 2001; 53(7):592-8. (Biology). View Reference
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Rozbeský D, Ivanova L, Hernychová L, Grobárová V, Novák P, Černý J. Nkrp1 family, from lectins to protein interacting molecules.. Molecules. 2015; 20(2):3463-78. (Biology). View Reference
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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.
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