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SYN1 抗体 (AA 662-705)

This anti-SYN1 antibody is a 兔 多克隆 antibody detecting SYN1 in WB 和 IHC (p). Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN5647272
发货至: 中国

Quick Overview for SYN1 抗体 (AA 662-705) (ABIN5647272)

抗原

See all SYN1 抗体
SYN1 (Synapsin I (SYN1))

适用

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人, 大鼠, 小鼠

宿主

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  • 8

克隆类型

  • 117
  • 17
多克隆

标记

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This SYN1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

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    • 1
    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    AA 662-705

    纯化方法

    Antigen affinity purified

    免疫原

    Amino acids 662-705 (KSQSLTNAFNLPEPAPPRPSLSQDEVKAETIRSLRKSFASLFSD) from the human protein were used as the immunogen for the Synapsin 1 antibody.

    亚型

    IgG
  • 应用备注

    Western blot: 0.5-1 μg/mL,IHC (FFPE): 1-2 μg/mL

    限制

    仅限研究用
  • 缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    -20 °C

    储存方法

    After reconstitution, the Synapsin 1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原

    SYN1 (Synapsin I (SYN1))

    别名

    Synapsin 1

    背景

    Synapsin I, is the collective name for Synapsin Ia and Synapsin Ib, two nearly identical phosphoproteins that in humans are encoded by the SYN1 gene. This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.

    UniProt

    P17600
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