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NA/LE Armenian hamster Anti-Mouse CD95 Recombinant mAb

Tumor necrosis factor receptor superfamily member 6,Apo-1 antigen,Apoptosis-mediating surface antigen FAS,FASLG receptor,Apt1,Tnfrsf6,Fas

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货号 S0E0025
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产品规格
  • 宿主来源

    Armenian hamster
  • 抗原名称

    CD95
  • 分子别名

    Tumor necrosis factor receptor superfamily member 6; Apo-1 antigen; Apoptosis-mediating surface antigen FAS; FASLG receptor; Apt1; Tnfrsf6; Fas
  • 细胞定位

    Cell membrane
  • Accession

    P25446
  • 克隆号

    S-R535
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    Armenian hamster IgG
  • 同型对照

    Invivo Armenian Hamster IgG Isotype Control
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse thymocytes
  • 纯化方式

    Protein G
  • 浓度

    5 mg/ml
  • 纯度

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

    <2EU/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

    Cytotoxicity

    in vivo cell specific stimulation/activation

    in vitro cell specific stimulation/activation

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1:200 Ms
背景介绍
  • CD95, also known as Fas or APO-1, is a 48 kDa type-I transmembrane receptor of the TNF-receptor superfamily that, upon trimerization by its cognate ligand CD95L (FasL), assembles the death-inducing signaling complex (DISC) by recruiting the adaptor FADD and procaspase-8/10, triggering a caspase cascade that culminates in apoptosis, thereby governing immune homeostasis, peripheral tolerance, and elimination of infected or oncogenic cells, while dysregulation of this pathway contributes to autoimmune lymphoproliferative syndrome, cancer immune evasion, and resistance to chemotherapy.

  • 流式分析

    • Flow cytometric analysis of BALB/c mouse thymocytes labelling Mouse CD95 antibody at 1/200 dilution (1 μg) / (Red) compared with a Armenian hamster monoclonal IgG (Black) isotype control followed by Anti-Armenian Hamster IgG (H+L) biotin and Sav-PE. Cells without incubation with primary antibody and secondary antibody (Blue) was used as unlabelled control.

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