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SYN1 anticorps

L’anticorps Lapin Polyclonal anti-SYN1 a été validé pour WB et ELISA. Il convient pour détecter SYN1 dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN7238405

Aperçu rapide pour SYN1 anticorps (ABIN7238405)

Antigène

Voir toutes SYN1 Anticorps
SYN1 (Synapsin I (SYN1))

Reactivité

  • 109
  • 87
  • 65
  • 15
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 118
  • 8
Lapin

Clonalité

  • 109
  • 17
Polyclonal

Conjugué

  • 79
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SYN1 est non-conjugé

Application

  • 91
  • 46
  • 42
  • 21
  • 13
  • 13
  • 11
  • 10
  • 10
  • 7
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Synthetic peptide of human SYN1

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    SYN1 (Synapsin I (SYN1))

    Autre désignation

    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

    74 kDa

    NCBI Accession

    NP_008881

    UniProt

    P17600
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