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SYN1 抗体

SYN1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2433199
发货至: 中国
  • 抗原 See all SYN1 抗体
    SYN1 (Synapsin I (SYN1))
    适用
    • 118
    • 95
    • 76
    • 16
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    宿主
    • 124
    • 7
    克隆类型
    • 116
    • 15
    多克隆
    标记
    • 77
    • 7
    • 6
    • 6
    • 6
    • 6
    • 6
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This SYN1 antibody is un-conjugated
    应用范围
    • 88
    • 44
    • 31
    • 20
    • 16
    • 13
    • 13
    • 7
    • 7
    • 7
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human SYN1
    亚型
    IgG
    Top Product
    Discover our top product SYN1 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.4 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    储存液
    Sodium azide
    注意事项
    Avoid freeze / thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SYN1 (Synapsin I (SYN1))
    别名
    SYN1 (SYN1 产品)
    别名
    SYN1a antibody, SYN1b antibody, SYNI antibody, Syn-1 antibody, SYN I antibody, si:dkey-90n12.3 antibody, synapsin I antibody, synapsin I L homeolog antibody, SYN1 antibody, Syn1 antibody, syn1.L antibody, syn1 antibody
    背景
    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.
    分子量
    Calculated MW: 74 kDa
    NCBI登录号
    NP_008881
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