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Nesprin3 antibody

C14orf49 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7256734
  • Target See all Nesprin3 (C14orf49) Antibodies
    Nesprin3 (C14orf49) (Chromosome 14 Open Reading Frame 49 (C14orf49))
    Reactivity
    • 41
    • 33
    • 16
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 41
    Rabbit
    Clonality
    • 41
    Polyclonal
    Conjugate
    • 17
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Nesprin3 antibody is un-conjugated
    Application
    • 41
    • 18
    • 13
    • 13
    • 13
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SYNE3 (NP_689805.3).
    Isotype
    IgG
    Top Product
    Discover our top product C14orf49 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Nesprin3 (C14orf49) (Chromosome 14 Open Reading Frame 49 (C14orf49))
    Alternative Name
    SYNE3 (C14orf49 Products)
    Synonyms
    C14orf49 antibody, NET53 antibody, Nesp3 antibody, 4831426I19Rik antibody, nesprin-3 antibody, spectrin repeat containing nuclear envelope family member 3 antibody, spectrin repeat containing, nuclear envelope family member 3 antibody, SYNE3 antibody, Syne3 antibody
    Background
    SYNE3 (Spectrin Repeat Containing Nuclear Envelope Family Member 3) is a Protein Coding gene. Diseases associated with SYNE3 include Spinocerebellar Ataxia, Autosomal Recessive 8 and Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive. Gene Ontology (GO) annotations related to this gene include actin binding and actin filament binding. An important paralog of this gene is SPTBN2.
    Molecular Weight

    Observed_MW: 112 kDa

    Calculated_MW: 68 kDa/111 kDa/112 kDa

    Gene ID
    161176
    UniProt
    Q6ZMZ3
    Pathways
    Maintenance of Protein Location
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