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SYN1 antibody

SYN1 Reactivity: Human WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2433199
  • Target See all SYN1 Antibodies
    SYN1 (Synapsin I (SYN1))
    Reactivity
    • 118
    • 95
    • 76
    • 16
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 124
    • 7
    Rabbit
    Clonality
    • 116
    • 15
    Polyclonal
    Conjugate
    • 77
    • 7
    • 6
    • 6
    • 6
    • 6
    • 6
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This SYN1 antibody is un-conjugated
    Application
    • 88
    • 44
    • 31
    • 20
    • 16
    • 13
    • 13
    • 7
    • 7
    • 7
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human SYN1
    Isotype
    IgG
    Top Product
    Discover our top product SYN1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SYN1 (Synapsin I (SYN1))
    Alternative Name
    SYN1 (SYN1 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    Calculated MW: 74 kDa
    NCBI Accession
    NP_008881
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