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PEX1 Antikörper (Middle Region)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch PEX1 in WB und EIA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN954094

Kurzübersicht für PEX1 Antikörper (Middle Region) (ABIN954094)

Target

Alle PEX1 Antikörper anzeigen
PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Reaktivität

  • 30
  • 9
  • 3
  • 1
  • 1
Human

Wirt

  • 29
  • 3
  • 1
Kaninchen

Klonalität

  • 32
  • 1
Polyklonal

Konjugat

  • 20
  • 4
  • 3
  • 3
  • 2
  • 1
Dieser PEX1 Antikörper ist unkonjugiert

Applikation

  • 21
  • 20
  • 9
  • 5
  • 3
  • 2
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Bindungsspezifität

    • 8
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 606-637, Middle Region

    Spezifität

    This antibody recognizes Human Peroxin 1 / PEX1 (Center).

    Aufreinigung

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 606-637 amino acids from the Central region of Human Peroxin 1 / PEX1

    Isotyp

    Ig Fraction
  • 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

    PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

    Andere Bezeichnung

    Peroxin 1 / PEX1

    Hintergrund

    This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.Synonyms: Peroxin-1, Peroxisome biogenesis disorder protein 1, Peroxisome biogenesis factor 1

    Molekulargewicht

    142867 Da

    Gen-ID

    5189

    NCBI Accession

    NP_000457
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