产品中心 药物靶点和Fc受体 药物靶点

所有图片(1/1)

Annexin A1 His Tag Protein, Human

Annexin I,Annexin-1,Calpactin II,Calpactin-2,Chromobindin-9

价格 1,150.00 1-2周
货号 UA106006
规格
数量
收藏 分享

产品介绍 评论(0)

产品规格
  • 物种

    Human
  • 分子别名

    Annexin I, Annexin-1, Calpactin II, Calpactin-2, Chromobindin-9
  • Accession

    P04083
  • 表达序列

    Ala2-Asn346 with C-10*His

  • 表达宿主

    E.coli
  • 分子量

    Theoretical: 40.4kDa Actual: 40kDa

  • 纯度

    >95% by SDS-PAGE
  • 内毒素含量

    <1EU/μg
  • 标记

    Unconjugated
  • 标签

    His Tag
  • 性状

    Lyophilized Powder
  • 溶解方法

    Reconstitute no more than 1 mg/mL according to the size in deionized water after rapid centrifugation.

  • 储存条件

    12 months from date of receipt, -20 to -70 °C as supplied.
    6 months, -20 to -70 °C under sterile conditions after reconstitution.
    1 week, 2 to 8 °C under sterile conditions after reconstitution.
    Please avoid repeated freeze-thaw cycles.

背景介绍
  • Annexin A1 belongs to the annexin family of Ca2+-dependent phospholipid-binding proteins. Annexin A1 has important opposing properties during innate and adaptive immune responses: it inhibits innate immune cells and promotes T-cell activation. The activation of T cells results in the release of annexin A1 and the expression of its receptor. This pathway seems to fine-tune the strength of TCR signalling. Higher expression of annexin A1 during pathological conditions could increase the strength of TCR signalling through the mitogen-activated protein kinase signalling pathway, thereby causing a state of hyperactivation of T cells. Annexin A1 has also been of interest for use as a potential anticancer drug. Upon induction by modified NSAIDS and other potent anti-inflammatory drugs, annexin A1 inhibits the NF-κB signal transduction pathway, which is exploited by cancerous cells to proliferate and avoid apoptosis. ANXA1 inhibits the activation of NF-κB by binding to the p65 subunit.

  • 电泳

    • 2μg(R: reducing conditions)

评论(0)