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SYN1 anticorps

SYN1 Reactivité: Humain WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2433199
  • Antigène Voir toutes SYN1 Anticorps
    SYN1 (Synapsin I (SYN1))
    Reactivité
    • 117
    • 95
    • 76
    • 16
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    Humain
    Hôte
    • 123
    • 7
    Lapin
    Clonalité
    • 115
    • 15
    Polyclonal
    Conjugué
    • 76
    • 7
    • 6
    • 6
    • 6
    • 6
    • 6
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SYN1 est non-conjugé
    Application
    • 87
    • 44
    • 31
    • 20
    • 16
    • 13
    • 13
    • 7
    • 7
    • 7
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human SYN1
    Isotype
    IgG
    Top Product
    Discover our top product SYN1 Anticorps primaire
  • Indications d'application
    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
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    SYN1 (Synapsin I (SYN1))
    Autre désignation
    SYN1 (SYN1 Produits)
    Synonymes
    anticorps SYN1a, anticorps SYN1b, anticorps SYNI, anticorps Syn-1, anticorps SYN I, anticorps si:dkey-90n12.3, anticorps synapsin I, anticorps synapsin I L homeolog, anticorps SYN1, anticorps Syn1, anticorps syn1.L, anticorps syn1
    Sujet
    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.
    Poids moléculaire
    Calculated MW: 74 kDa
    NCBI Accession
    NP_008881
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