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PEX12 antibody (Middle Region)

PEX12 Reactivity: Human, Mouse WB, EIA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN954095
  • Target See all PEX12 Antibodies
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Binding Specificity
    • 8
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 137-167, Middle Region
    Reactivity
    • 18
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 14
    • 3
    • 1
    Rabbit
    Clonality
    • 16
    • 2
    Polyclonal
    Conjugate
    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    This PEX12 antibody is un-conjugated
    Application
    • 15
    • 13
    • 1
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Specificity
    This antibody recognizes Human and Mouse Peroxin 12 / PEX12 (Center).
    Purification
    Protein A column, followed by peptide affinity purification
    Immunogen
    KLH conjugated synthetic peptide between 137~167 amino acids from the Central region of human PEX12
    Isotype
    Ig Fraction
    Top Product
    Discover our top product PEX12 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.25 mg/mL
    Buffer
    PBS containing 0.09 % (W/V) Sodium Azide as preservative
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Alternative Name
    Peroxin 12 / PEX12 (PEX12 Products)
    Background
    Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle.Synonyms: PAF-3, PAF3, Peroxin-12, Peroxisome assembly factor 3, Peroxisome assembly protein 12
    Molecular Weight
    40797 Da
    Gene ID
    5193
    NCBI Accession
    NP_000277
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