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FITC Mouse Anti-Mouse Ly-49H
FITC Mouse Anti-Mouse Ly-49H
Multicolor flow cytometric analysis of Ly-49H expression on BALB/c and C57BL/6 splenocytes. Mouse spleen cells from BALB/c (Left Panel) or C57BL/6 (Right Panel) mice were stained with FITC Mouse Anti-Mouse Ly-49H (Cat. No. 562536) and APC Rat Anti-Mouse CD49b (Clone DX5, Cat. No. 560628) antibodies. Two-color flow cytometric dot plots showing the correlated expression patterns of CD49b versus Ly-49H were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. As expected, only C57BL/6 mouse splenocytes contained a subset of NK cells (Right Panel) that expressed Ly-49H whereas BALB/c splenocytes were Ly-49H-negative (Left Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multicolor flow cytometric analysis of Ly-49H expression on BALB/c and C57BL/6 splenocytes. Mouse spleen cells from BALB/c (Left Panel) or C57BL/6 (Right Panel) mice were stained with FITC Mouse Anti-Mouse Ly-49H (Cat. No. 562536) and APC Rat Anti-Mouse CD49b (Clone DX5, Cat. No. 560628) antibodies. Two-color flow cytometric dot plots showing the correlated expression patterns of CD49b versus Ly-49H were derived from gated events with the forward and side light-scatter characteristics of viable splenocytes. As expected, only C57BL/6 mouse splenocytes contained a subset of NK cells (Right Panel) that expressed Ly-49H whereas BALB/c splenocytes were Ly-49H-negative (Left Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
製品詳細
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BD Pharmingen™
Ly49h; Lymphocyte antigen 49H; Klra8; Cmv1; Cmv-1
Mouse (QC Testing)
Mouse BALB/c IgG1, κ
Mouse Ly-49A/H Transfected Cell Line
Flow cytometry (Routinely Tested)
0.5 mg/ml
16639
AB_2737638
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 with FITC under optimum conditions, and unreacted FITC was removed.

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. An isotype control should be used at the same concentration as the antibody of interest.
  3. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  4. 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.
  5. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
562536 Rev. 1
抗体の詳細
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3D10

The 3D10 monoclonal antibody specifically binds to mouse Lymphocyte antigen 49H (Ly-49H; also known as Klra8 or Killer cell lectin-like receptor 8). The 3D10 antibody does not crossreact with related molecules such as Ly-49A, C, D or G2. Ly-49H is a type II transmembrane protein and a member of the Ly-49 C-type lectin multigene family of receptors expressed by NK cells. Cell surface Ly-49H is expressed by a subset of NK cells but not by NKT cells. Ly-49H is expressed by C57BL/6 and NWNA but not by BALB/c or DBA/2 mouse NK cells. Cell surface Ly-49H presents as a ~110 kDa disfulfide-linked homodimer and associates with signaling subunits such as DAP10 and DAP12 for optimal transduction of intracellular activation signals. Crosslinking of Ly-49H with the 3D10 antibody reportedly induces NK cell cytotoxicity and cytokine production. Ly-49H recognizes the mouse cytomegalovirus m157 glycoprotein that is expressed by infected cells and is required for protection against cytomegalovirus infection.

562536 Rev. 1
フォーマットの詳細
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FITC
Fluorescein (FITC) is part of the BD blue family of dyes. This is a small organic fluorochrome with an excitation maximum (Ex Max) at 494-nm and an emission maximum (Em Max) at 518-nm. FITC is designed to be excited by the Blue laser (488-nm) and detected using an optical filter centered near 520 nm (e.g., a 530/30-nm bandpass filter). Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
altImg
FITC
Blue 488 nm
494 nm
518 nm
562536 Rev.1
引用&参考文献
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Development References (5)

  1. Brennan J, Mager D, Jefferies W, Takei F. Expression of different members of the Ly-49 gene family defines distinct natural killer cell subsets and cell adhesion properties. J Exp Med. 1994; 180(6):2287-2295. (Biology). View Reference
  2. Brown MG, Dokun AO, Heusel JW, et al. Vital involvement of a natural cell activation receptor in resistance to viral infection. Science. 2001; 292(5518):934-937. (Clone-specific: Activation, Bioassay, Blocking, Cytotoxicity, Flow cytometry). View Reference
  3. Orr MT, Sun JC, Hesslein DG, et al. Ly49H signaling through DAP10 is essential for optimal natural killer cell responses to mouse cytomegalovirus infection. J Exp Med. 2009; 206(4):807-817. (Clone-specific: Blocking, Flow cytometry). View Reference
  4. Silver ET, Elliott JF, Kane KP. Alternatively spliced Ly-49D and H transcripts are found in IL-2-activated NK cells. Immunogenetics. 1996; 44(6):478-482. (Biology). View Reference
  5. Smith HR, Chuang HH, Wang LL, Salcedo M, Heusel JW, Yokoyama WM. Nonstochastic Coexpression of activation receptors on murine Natural Killer cells. J Exp Med. 2000; 191(8):1341-1354. (Immunogen: Activation, Cytotoxicity, Flow cytometry, Immunoprecipitation). View Reference
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562536 Rev. 1

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For Research Use Only. Not for use in diagnostic or therapeutic procedures.