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Amyloid beta 1-42 Recombinant Rabbit mAb (SDT-1549-98)

货号: S0B3396

Datasheet COA
  • 价格: 询价
  • 规格:
  • 数量:
斯达特大包装询价 大包装询价

产品介绍 引用文献(0) 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Amyloid beta 1-40
  • 分子别名

    Aβ1-42
  • 免疫原

    Synthetic Peptide
  • Accession

    P05067
  • 克隆号

    SDT-1549-98
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    Sandwich ELISA
  • 反应种属 ?

    Hu, Ms
  • 交叉反应

    No cross-reactivity against with Amyloid beta 1-40

  • 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 / reconstitution, 2 to 8 °C as supplied

  • 稀释度

    [{"application": "ELISA", "dilution": "", "species": ""}, {"application": "Sandwich ELISA", "dilution": "", "species": ""}, {"application": "CLIA", "dilution": "", "species": ""}, {"application": "Lateral Flow", "dilution": "", "species": ""}, {"application": "Dot Blot", "dilution": "", "species": ""}, {"application": "WB", "dilution": "", "species": ""}, {"application": "IP", "dilution": "", "species": ""}, {"application": "IHC-P", "dilution": "", "species": ""}, {"application": "ICC", "dilution": "", "species": ""}, {"application": "IF", "dilution": "", "species": ""}, {"application": "ICFCM", "dilution": "", "species": ""}, {"application": "FCM", "dilution": "", "species": ""}, {"application": "mIHC", "dilution": "", "species": ""}]
背景介绍
  • Amyloid beta 1-42 (Aβ1-42) is a peptide composed of 42 amino acids, derived from the enzymatic cleavage of the amyloid precursor protein (APP). It is the primary component of amyloid plaques in Alzheimer's disease (AD) and is highly hydrophobic and prone to aggregation. Aβ1-42 is more likely than the more common Aβ1-40 to form toxic oligomers and fibrils, which are believed to play a key role in the pathological process of AD by disrupting neuronal function, triggering inflammatory responses, and causing synaptic dysfunction. The abnormal accumulation and aggregation of Aβ1-42 is one of the early pathological hallmarks of AD and a critical target for research and treatment of the disease.

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