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PEX10 antibody

PEX10 Reactivity: Human, Mouse, Rat IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7009572
  • Target See all PEX10 Antibodies
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Reactivity
    • 24
    • 17
    • 3
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 37
    • 2
    Rabbit
    Clonality
    • 37
    • 2
    Polyclonal
    Conjugate
    • 15
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This PEX10 antibody is un-conjugated
    Application
    • 14
    • 13
    • 13
    • 13
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human PEX10 (NP_002608.1).
    Isotype
    IgG
    Top Product
    Discover our top product PEX10 Primary Antibody
  • Application Notes
    IF 1:50-1:200
    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
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Alternative Name
    PEX10 (PEX10 Products)
    Synonyms
    ATPEX10 antibody, T9J22.2 antibody, peroxin 10 antibody, NALD antibody, PBD6A antibody, PBD6B antibody, RNF69 antibody, AV128229 antibody, Gm142 antibody, peroxin 10 antibody, peroxisomal biogenesis factor 10 antibody, PEX10 antibody, Pex10 antibody
    Background
    This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.
    Gene ID
    5192
    UniProt
    O60683
    Pathways
    Monocarboxylic Acid Catabolic Process
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