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Neurexin 1 抗体 (AA 77-110)

This 兔 多克隆 antibody specifically detects Neurexin 1 in WB. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN7876757
发货至: 中国
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Quick Overview for Neurexin 1 抗体 (AA 77-110) (ABIN7876757)

抗原

See all Neurexin 1 (NRXN1) 抗体
Neurexin 1 (NRXN1)

适用

人, 大鼠, 小鼠

宿主

  • 21
  • 9
  • 1
  • 1

克隆类型

  • 24
  • 8
多克隆

标记

  • 23
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Neurexin 1 antibody is un-conjugated

应用范围

  • 22
  • 17
  • 7
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 8
    • 8
    • 6
    • 6
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 77-110

    原理

    NRXN1 Antibody / Neurexin 1 beta

    纯化方法

    Antigen affinity

    免疫原

    A portion of amino acids 77-110 from the human protein was used as the immunogen for this NRXN1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    The stated application concentrations are suggested starting amounts. Titration of the NRXN1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Store at 4oC for up to one month. For long term, aliquot the NRXN1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    Neurexin 1 (NRXN1)

    别名

    NRXN1

    背景

    Neurexin 1 is primarily known for its role in the formation and maintenance of synapses, the connections between neurons that allow for communication in the brain. It acts as a cell adhesion molecule, helping to guide the development of synapses and ensuring proper signaling between neurons. Studies have shown that mutations in the NRXN1 gene can lead to disruptions in synaptic function, ultimately impacting brain development and function. These mutations have been associated with a variety of neurological disorders, including autism spectrum disorder, schizophrenia, and intellectual disabilities.

    UniProt

    P58400

    途径

    Synaptic Membrane, Skeletal Muscle Fiber Development
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