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PE Mouse Anti-Mouse CD369 (Clec7a)
PE Mouse Anti-Mouse CD369 (Clec7a)
Flow Cytometric Analysis of CD369 (Clec7a) Expression    Top plots - CD369 (Clec7a) expression on Mouse peripheral blood leucocytes (PBL): BALB/c (Panel 1) and C57BL/6 (Panel 2) mouse peripheral blood leucocytes (PBL) were stained with APC Rat Anti-Mouse Ly-6G antibody (Cat. No. 560599) and with either PE mouse IgG1, κ Isotype Control (Cat. No. 550083; Plots A&C) or PE Mouse Anti-Mouse CD369 (Clec7a) antibody (Cat. No. 568714; Plots B&D) at 1.0 ug/test. The bivariate pseudocolor density plots showing the correlated expression of CD369 (Clec7a) [or Ig isotype control staining] versus Ly-6G were derived from gated events with the forward and side-light scatter characteristics of viable leucocyte populations.    Bottom plots - CD369 (Clec 7a) expression on Mouse peritoneal exudate cells (PEC): BALB/c (Panel 1) and C57BL/6 (Panel 2) mouse thioglycolate-elicited PEC cells. were harvested and pre-incubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) [Cat. No. 553141/553142]. The cells were then stained with Alexa Fluor™ Rat Anti-Mouse F4/80 antibody (Cat. No. 565854) and with either PE mouse IgG1, κ Isotype Control (Cat. No. 550083; Plots E&G) or PE Mouse Anti-Mouse CD369 (Clec7a) antibody (Cat. No. 568714; Plots F&H) at 1.0 ug/test. The bivariate pseudocolor density plots showing the correlated expression of CD369 (Clec7a) [or Ig isotype control staining] versus F4/80 were derived from gated events with the forward and side-light scatter characteristics of viable PEC cells.    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 CD369 (Clec7a) Expression    Top plots - CD369 (Clec7a) expression on Mouse peripheral blood leucocytes (PBL): BALB/c (Panel 1) and C57BL/6 (Panel 2) mouse peripheral blood leucocytes (PBL) were stained with APC Rat Anti-Mouse Ly-6G antibody (Cat. No. 560599) and with either PE mouse IgG1, κ Isotype Control (Cat. No. 550083; Plots A&C) or PE Mouse Anti-Mouse CD369 (Clec7a) antibody (Cat. No. 568714; Plots B&D) at 1.0 ug/test. The bivariate pseudocolor density plots showing the correlated expression of CD369 (Clec7a) [or Ig isotype control staining] versus Ly-6G were derived from gated events with the forward and side-light scatter characteristics of viable leucocyte populations.    Bottom plots - CD369 (Clec 7a) expression on Mouse peritoneal exudate cells (PEC): BALB/c (Panel 1) and C57BL/6 (Panel 2) mouse thioglycolate-elicited PEC cells. were harvested and pre-incubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) [Cat. No. 553141/553142]. The cells were then stained with Alexa Fluor™ Rat Anti-Mouse F4/80 antibody (Cat. No. 565854) and with either PE mouse IgG1, κ Isotype Control (Cat. No. 550083; Plots E&G) or PE Mouse Anti-Mouse CD369 (Clec7a) antibody (Cat. No. 568714; Plots F&H) at 1.0 ug/test. The bivariate pseudocolor density plots showing the correlated expression of CD369 (Clec7a) [or Ig isotype control staining] versus F4/80 were derived from gated events with the forward and side-light scatter characteristics of viable PEC cells.    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.
製品詳細
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BD Pharmingen™
Clec7a; CD369; BGR; Beta-glucan receptor; Bgr; Dectin-1; Dectin1; dectin-1
Mouse (QC Testing)
Mouse BALB/c IgG1, κ
Mouse Dectin-1 Recombinant Protein
Flow cytometry (Routinely Tested)
0.2 mg/ml
56644
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation and Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to the dye under optimum conditions and unconjugated antibody and free dye were removed.

推奨アッセイ手順

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.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. 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.
  3. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  4. An isotype control should be used at the same concentration as the antibody of interest.
  5. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  6. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
568714 Rev. 1
抗体の詳細
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2F3

The 2F3 monoclonal antibody specifically recognizes CD369 which is also known as Dectin-1 (Dendritic cell-associated C-type lectin 1) or BGR (Beta-glucan receptor). CD369 is a ~ 43 kDa type II transmembrane C-type lectin that is encoded by Clec7a (C-type lectin domain family 7, member a). The extracellular portion of CD369 (Clec7a) contains a C-terminal stalk with a carbohydrate recognition domain (CRD) that is followed by a transmembrane segment, and an ITAM-containing cytoplasmic tail. This protein is predominantly expressed on monocytes/macrophages, neutrophils and some dendritic cell populations and at a lower level on a sub-population of T cells. CD369 (Clec7a) binds to beta-glucan polymers and functions as a pattern recognition receptor (PRR) in innate immune response to fungal and bacterial pathogens. CD369 mediated signaling may play a role in leucocyte responses, including phagocytosis or enhanced cytokine production. In mice, two functionally different full-length and stalkless isoforms have been characterized. Both isoforms vary in their ability to recognize zymosan and mediate cellular responses upon zymosan recognition.

568714 Rev. 1
フォーマットの詳細
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PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
altImg
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
568714 Rev.1
引用&参考文献
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Development References (4)

  1. Brown GD, Taylor PR, Reid DM, et al. Dectin-1 is a major beta-glucan receptor on macrophages.. J Exp Med. 2002; 196(3):407-12. (Biology). View Reference
  2. Herre J, Gordon S, Brown GD. Dectin-1 and its role in the recognition of beta-glucans by macrophages.. Mol Immunol. 2004; 40(12):869-76. (Biology). View Reference
  3. Taylor PR, Brown GD, Reid DM, et al. The beta-glucan receptor, dectin-1, is predominantly expressed on the surface of cells of the monocyte/macrophage and neutrophil lineages.. J Immunol. 2002; 169(7):3876-82. (Biology). View Reference
  4. Underhill DM, Rossnagle E, Lowell CA, Simmons RM. Dectin-1 activates Syk tyrosine kinase in a dynamic subset of macrophages for reactive oxygen production.. Blood. 2005; 106(7):2543-50. (Biology). View Reference
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568714 Rev. 1

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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.