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CD69 抗体 (Biotin)

This anti-CD69 antibody is a Armenian Hamster 单克隆 antibody detecting CD69 in FACS. Suitable for 小鼠. This Primary Antibody has been cited in 15+ publications.
产品编号 ABIN2689380
发货至: 中国

Quick Overview for CD69 抗体 (Biotin) (ABIN2689380)

抗原

See all CD69 抗体
CD69

适用

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小鼠

宿主

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Armenian Hamster

克隆类型

  • 80
  • 58
单克隆

标记

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This CD69 antibody is conjugated to Biotin

应用范围

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Flow Cytometry (FACS)

克隆位点

H1-2F3
  • 品牌

    BD Pharmingen™

    产品特性

    The H1.2F3 antibody reacts with CD69 (Very Early Activation antigen), an 85 kDa disulfide-linked homodimer of differentially glycosylated subunits. CD69 is a C-type lectin, most closely related to the NKR-P1 and Ly-49 NK cell-activation molecules. Its expression is rapidly induced upon activation of lymphocytes (T, B, NK, and NK-T cells), neutrophils, and macrophages. CD69 is expressed also on thymocytes that are undergoing positive selection, its role in that process is unclear. H1.2F3 mAb augments PMA-induced T-cell stimulation and IFN-γ-induced macrophage stimulation. IL-2-activated NK cells express CD69, and H1.2F3 mAb induces redirected lysis of FcR-bearing target cells by NK cells. This antibody is routinely tested by flow cytometric analysis. Other applications were tested during antibody development only or reported in the literature.

    BD Pharmingen™ Biotin Hamster Anti-Mouse CD69 - Biotin - Clone H1.2F3 - Isotype Armenian Hamster IgG1, λ3 - Reactivity Ms - 0.5 mg

    纯化方法

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    免疫原

    Mouse Dendritic Epidermal T Cell Line Y245

    亚型

    IgG1 lambda
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 浓度

    0.5 mg/mL

    缓冲液

    Aqueous buffered solution containing ≤0.09 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    The antibody was conjugated with biotin under optimum conditions, and unreacted biotin was removed.

    储存条件

    4 °C

    储存方法

    Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.
  • Lauzurica, Sancho, Torres, Albella, Marazuela, Merino, Bueren, Martínez-A, Sánchez-Madrid: "Phenotypic and functional characteristics of hematopoietic cell lineages in CD69-deficient mice." in: Blood, Vol. 95, Issue 7, pp. 2312-20, (2000) (PubMed).

    Keefe, Dave, Allman, Wiest, Kappes: "Regulation of lineage commitment distinct from positive selection." in: Science (New York, N.Y.), Vol. 286, Issue 5442, pp. 1149-53, (1999) (PubMed).

    Gabor, Godfrey, Scollay: "Recent thymic emigrants are distinct from most medullary thymocytes." in: European journal of immunology, Vol. 27, Issue 8, pp. 2010-5, (1997) (PubMed).

    Marzio, Jirillo, Ransijn, Mauël, Corradin: "Expression and function of the early activation antigen CD69 in murine macrophages." in: Journal of leukocyte biology, Vol. 62, Issue 3, pp. 349-55, (1997) (PubMed).

    Merkenschlager, Graf, Lovatt, Bommhardt, Zamoyska, Fisher: "How many thymocytes audition for selection?" in: The Journal of experimental medicine, Vol. 186, Issue 7, pp. 1149-58, (1997) (PubMed).

    Punt, Suzuki, Granger, Sharrow, Singer: "Lineage commitment in the thymus: only the most differentiated (TCRhibcl-2hi) subset of CD4+CD8+ thymocytes has selectively terminated CD4 or CD8 synthesis." in: The Journal of experimental medicine, Vol. 184, Issue 6, pp. 2091-9, (1997) (PubMed).

    Wilkinson, Anderson, Owen, Jenkinson: "Positive selection of thymocytes involves sustained interactions with the thymic microenvironment." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 155, Issue 11, pp. 5234-40, (1995) (PubMed).

    Ziegler, Ramsdell, Alderson: "The activation antigen CD69." in: Stem cells (Dayton, Ohio), Vol. 12, Issue 5, pp. 456-65, (1995) (PubMed).

    Brändle, Müller, Müller, Hengartner, Pircher: "Regulation of RAG-1 and CD69 expression in the thymus during positive and negative selection." in: European journal of immunology, Vol. 24, Issue 1, pp. 145-51, (1994) (PubMed).

    Ziegler, Levin, Johnson, Copeland, Gilbert, Jenkins, Baker, Sutherland, Feldhaus, Ramsdell: "The mouse CD69 gene. Structure, expression, and mapping to the NK gene complex." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 152, Issue 3, pp. 1228-36, (1994) (PubMed).

    Sobel, Yokoyama, Shevach, Eisenberg, Cohen: "Aberrant expression of the very early activation antigen on MRL/Mp-lpr/lpr lymphocytes." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 150, Issue 2, pp. 673-82, (1993) (PubMed).

    Bendelac, Matzinger, Seder, Paul, Schwartz: "Activation events during thymic selection." in: The Journal of experimental medicine, Vol. 175, Issue 3, pp. 731-42, (1992) (PubMed).

    Karlhofer, Yokoyama: "Stimulation of murine natural killer (NK) cells by a monoclonal antibody specific for the NK1.1 antigen. IL-2-activated NK cells possess additional specific stimulation pathways." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 146, Issue 10, pp. 3662-73, (1991) (PubMed).

    Yokoyama, Maxfield, Shevach: "Very early (VEA) and very late (VLA) activation antigens have distinct functions in T lymphocyte activation." in: Immunological reviews, Vol. 109, pp. 153-76, (1989) (PubMed).

    Yokoyama, Koning, Kehn, Pereira, Stingl, Coligan, Shevach: "Characterization of a cell surface-expressed disulfide-linked dimer involved in murine T cell activation." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 141, Issue 2, pp. 369-76, (1988) (PubMed).

  • 抗原

    CD69

    别名

    CD69

    背景

    Synonyms: Very Early Activation antigen
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