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S100A12 Recombinant Rabbit mAb (SDT-2776-55)

Protein S100-A12,CGRP,Calcium-binding protein in amniotic fluid 1 (CAAF1),Calgranulin-C (CAGC),Extracellular newly identified RAGE-binding protein (EN-RAGE),Migration inhibitory factor-related protein 6 (MRP-6,p6),S100A12

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货号 S0B3704
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    S100A12
  • 分子别名

    Protein S100-A12; CGRP; Calcium-binding protein in amniotic fluid 1 (CAAF1); Calgranulin-C (CAGC); Extracellular newly identified RAGE-binding protein (EN-RAGE); Migration inhibitory factor-related protein 6 (MRP-6; p6); S100A12
  • 免疫原

    Recombinant Protein
  • Accession

    P80511
  • 克隆号

    SDT-2776-55
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu
  • 交叉反应

    No cross-reactivity against S100A4

  • 纯化方式

    Protein A
  • 浓度

    2 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, 0.03% Proclin 300

  • 储存条件

    12 months from date of receipt, 2 to 8 °C as supplied

  • 应用

    Sandwich ELISA

背景介绍
  • S100A12, a calcium-binding protein primarily expressed in granulocytes, has emerged as a promising biomarker for Alzheimer’s disease (AD), offering significant diagnostic value beyond traditional markers. Unlike amyloid-beta or tau proteins, which reflect core AD pathology but often require invasive cerebrospinal fluid (CSF) sampling or expensive PET imaging, S100A12 can be detected in peripheral blood, providing a less invasive and more accessible diagnostic tool.

    Research indicates that S100A12 levels are significantly elevated in the blood and brain tissues of AD patients compared to healthy controls. This elevation correlates with neuroinflammation, a critical driver of AD progression. S100A12 activates the receptor for advanced glycation end products (RAGE), triggering inflammatory cascades that exacerbate neuronal damage and cognitive decline. Consequently, high S100A12 levels not only aid in distinguishing AD from other dementias but also potentially reflect disease severity and activity.

    The diagnostic significance lies in its ability to detect early-stage inflammation before substantial neurodegeneration occurs. When combined with existing biomarkers, S100A12 improves diagnostic accuracy and sensitivity. Furthermore, monitoring S100A12 dynamics could help track therapeutic responses to anti-inflammatory treatments. While further large-scale clinical validation is needed, S100A12 represents a valuable, cost-effective addition to the AD diagnostic arsenal, facilitating earlier intervention and better management of this devastating neurodegenerative disorder through a simple blood test.

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