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PEX12 Antikörper (Middle Region)

PEX12 Reaktivität: Human, Maus WB, EIA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN954095
  • Target Alle PEX12 Antikörper anzeigen
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Bindungsspezifität
    • 8
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 137-167, Middle Region
    Reaktivität
    • 18
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 14
    • 3
    • 1
    Kaninchen
    Klonalität
    • 16
    • 2
    Polyklonal
    Konjugat
    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    Dieser PEX12 Antikörper ist unkonjugiert
    Applikation
    • 15
    • 13
    • 1
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Spezifität
    This antibody recognizes Human and Mouse Peroxin 12 / PEX12 (Center).
    Aufreinigung
    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
    Isotyp
    Ig Fraction
    Top Product
    Discover our top product PEX12 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.25 mg/mL
    Buffer
    PBS containing 0.09 % (W/V) Sodium Azide as preservative
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freezing and thawing.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Andere Bezeichnung
    Peroxin 12 / PEX12 (PEX12 Produkte)
    Hintergrund
    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
    Molekulargewicht
    40797 Da
    Gen-ID
    5193
    NCBI Accession
    NP_000277
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