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Invivo anti-Mouse CD24 Recombinant mAb

Signal transducer CD24,Lymphocyte antigen 52 (Ly-52),M1/69-J11D heat stable antigen (HSA),Nectadrin,R13-Ag,X62 heat stable antigen,Cd24a,Ly-52,Cd24

价格 1,050.00 供应商现货 : 3-5个工作日
货号 S0B7107
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD24
  • 分子别名

    Signal transducer CD24; Lymphocyte antigen 52 (Ly-52); M1/69-J11D heat stable antigen (HSA); Nectadrin; R13-Ag; X62 heat stable antigen; Cd24a; Ly-52; Cd24
  • 细胞定位

    Cell membrane
  • Accession

    P24807
  • 克隆号

    M1/69
  • 抗体类型

    Rat mAb
  • 抗体同种型

    Rat IgG2b, κ
  • 同型对照

    Invivo rat IgG2b isotype control, anti-keyhole limpet hemocyanin
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 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 neutralization

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1:500 Ms
背景介绍
  • CD24, also known as the cluster of differentiation 24, is a highly glycosylated glycosylphosphatidylinositol (GPI)-anchored surface protein that plays crucial roles in various physiological and pathological processes. Initially identified as a B-cell differentiation antigen, it is widely expressed in hematopoietic stem cells, B and T lymphocytes, epithelial cells, and neural cells. Structurally, CD24 has an intracellular domain, a transmembrane domain, and a heavily glycosylated extracellular domain, which is involved in cell adhesion, migration, differentiation, and apoptosis.

  • 流式分析

    • Flow cytometric analysis of C57BL/6 mouse splenocytes labeled with Mouse CD24 antibody at 1/500 dilution (1 μg) / (right panel) compared with a Rat IgG2b, κ Isotype Control / (left panel). Goat Anti-Rat IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD3 - Brilliant Violet 421™ antibody separately. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.

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