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PEX1 anticorps (Middle Region)

Cet anticorps Lapin Polyclonal détecte spécifiquement PEX1 dans WB et EIA. Il présente une réactivité envers Humain.
N° du produit ABIN954094

Aperçu rapide pour PEX1 anticorps (Middle Region) (ABIN954094)

Antigène

Voir toutes PEX1 Anticorps
PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Reactivité

  • 30
  • 9
  • 3
  • 1
  • 1
Humain

Hôte

  • 29
  • 3
  • 1
Lapin

Clonalité

  • 32
  • 1
Polyclonal

Conjugué

  • 20
  • 4
  • 3
  • 3
  • 2
  • 1
Cet anticorp PEX1 est non-conjugé

Application

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

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

    Specificité

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

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogène

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

    Isotype

    Ig Fraction
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

    Autre désignation

    Peroxin 1 / PEX1

    Sujet

    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

    Poids moléculaire

    142867 Da

    ID gène

    5189

    NCBI Accession

    NP_000457
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