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SYN1 Antikörper

Der Kaninchen Polyklonal Anti-SYN1-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, SYN1 in Proben von Human, Ratte und Maus zu detektieren.
Produktnummer ABIN7238405

Kurzübersicht für SYN1 Antikörper (ABIN7238405)

Target

Alle SYN1 Antikörper anzeigen
SYN1 (Synapsin I (SYN1))

Reaktivität

  • 112
  • 92
  • 69
  • 15
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Ratte, Maus

Wirt

  • 126
  • 8
Kaninchen

Klonalität

  • 117
  • 17
Polyklonal

Konjugat

  • 87
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SYN1 Antikörper ist unkonjugiert

Applikation

  • 98
  • 49
  • 46
  • 24
  • 13
  • 13
  • 13
  • 12
  • 12
  • 7
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Synthetic peptide of human SYN1

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    SYN1 (Synapsin I (SYN1))

    Andere Bezeichnung

    SYN1

    Hintergrund

    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

    Molekulargewicht

    74 kDa

    NCBI Accession

    NP_008881

    UniProt

    P17600
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