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SYN1 antibody

The Rabbit Polyclonal anti-SYN1 antibody has been validated for WB and ELISA. It is suitable to detect SYN1 in samples from Human, Rat and Mouse.
Catalog No. ABIN7238405

Quick Overview for SYN1 antibody (ABIN7238405)

Target

See all SYN1 Antibodies
SYN1 (Synapsin I (SYN1))

Reactivity

  • 112
  • 92
  • 69
  • 15
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Rat, Mouse

Host

  • 126
  • 8
Rabbit

Clonality

  • 117
  • 17
Polyclonal

Conjugate

  • 87
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SYN1 antibody is un-conjugated

Application

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

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human SYN1

    Isotype

    IgG
  • Application Notes

    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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

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

    SYN1 (Synapsin I (SYN1))

    Alternative Name

    SYN1

    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

    74 kDa

    NCBI Accession

    NP_008881

    UniProt

    P17600
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