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ATP13A2 anticorps (PE)

Cet anticorps Lapin Polyclonal détecte spécifiquement ATP13A2 dans . Il présente une réactivité envers Humain, Rat et Souris.
N° du produit ABIN1427815

Aperçu rapide pour ATP13A2 anticorps (PE) (ABIN1427815)

Antigène

Voir toutes ATP13A2 Anticorps
ATP13A2 (ATPase Type 13A2 (ATP13A2))

Reactivité

  • 19
  • 17
  • 3
  • 1
Humain, Rat, Souris

Hôte

  • 31
  • 3
Lapin

Clonalité

  • 32
  • 2
Polyclonal

Conjugué

  • 14
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ATP13A2 est conjugé à/à la PE

Application

Veuillez nous consulter SVP
  • Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human ATP13A2

    Isotype

    IgG
  • Commentaires

    Exitation/Emission: 480,565nm/578nm

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 100 μg/mL BSA, 50 % glycerol and 0.09 % sodium azide.

    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.

    Stock

    -20 °C

    Stockage commentaire

    Store at 4°C

    Date de péremption

    12 months
  • Antigène

    ATP13A2 (ATPase Type 13A2 (ATP13A2))

    Autre désignation

    Park9/Atp13a2

    Sujet

    ATP13A2 is a 1,180 amino acid multi-pass membrane protein that belongs to the P5 subfamily of ATPases which play an important role in the transportation of inorganic cations. Expressed as multiple alternative spliced isoforms, ATP13A2 functions to catalyze the conversion of ATP to ADP and a free phosphate, thereby participating in the active transport of ions across cellular membranes. Defects in the gene encoding ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS), a rare hereditary type of Parkinson’s disease that exhibits juvenile onset and is characterized by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome.

    Subcellular location: Extracellular


    Synonyms: AT132_HUMAN, Atp13a2, ATPase type 13A2, CLN12, HSA9947, KRPPD, PARK9, Probable cation transporting ATPase 13A2, Probable cation-transporting ATPase 13A2, Putative ATPase, RP1-37C10.4.

    Pathways

    Ribonucleoside Biosynthetic Process
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