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Invivo Anti-Mouse ICOS Recombinant mAb

Inducible T-cell costimulator,Activation-inducible lymphocyte immunomediatory molecule,CD28 and CTLA-4-like protein (CCLP),CD28-related protein 1 (CRP-1),CD278,Ailim,Icos

价格 1,050.00 供应商现货 : 3-5个工作日
货号 S0B7060
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    ICOS
  • 分子别名

    Inducible T-cell costimulator; Activation-inducible lymphocyte immunomediatory molecule; CD28 and CTLA-4-like protein (CCLP); CD28-related protein 1 (CRP-1); CD278; Ailim; Icos
  • 细胞定位

    Cell membrane
  • Accession

    Q9WVS0
  • 克隆号

    7E.17G9
  • 抗体类型

    Rat mAb
  • 抗体同种型

    Rat IgG2b,k
  • 同型对照

    Invivo rat IgG2b isotype control, anti-keyhole limpet hemocyanin
  • 纯化方式

    Protein G
  • 浓度

    5 mg/ml
  • 纯度

    >95%(Determined by SDS-PAGE)
  • 内毒素含量

    <1EU/mg
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, containing no preservative

  • 储存条件

    2 to 8 °C for 2 weeks under sterile conditions;
    -20 °C for 3 months under sterile conditions;
    -80 °C for 24 months under sterile conditions.
    Please avoid repeated freeze-thaw cycles.

  • 应用

    in vivo blocking of ICOS/ICOSL signaling

    FCM

背景介绍
  • ICOS (inducible T-cell costimulator, CD278) is a 55–60 kDa disulfide-linked homodimeric CD28-superfamily receptor expressed mainly on activated CD4⁺ and CD8⁺ T cells, Th17, Tfh and some NK subsets; its surface engagement by the ligand ICOSL (B7-H2/CD275) on antigen-presenting cells delivers a critical secondary signal that amplifies PI3K–AKT–mTOR and MAPK cascades, enhances cytokine transcription (IL-4, IL-10, IL-17, IL-21, IFN-γ), stabilizes Tfh differentiation, germinal-center reactions and class-switch recombination, and promotes memory formation, whereas genetic loss or therapeutic blockade of ICOS attenuates autoimmune pathology in experimental allergic encephalomyelitis, lupus, colitis and graft-versus-host disease yet can dampen antitumor immunity, making the pathway a finely balanced target for both immunosuppressive and immunostimulatory clinical interventions.

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