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ATP13A2 Antikörper (PE)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ATP13A2 in . Er zeigt eine Reaktivität gegenüber Human, Ratte und Maus.
Produktnummer ABIN1427815

Kurzübersicht für ATP13A2 Antikörper (PE) (ABIN1427815)

Target

Alle ATP13A2 Antikörper anzeigen
ATP13A2 (ATPase Type 13A2 (ATP13A2))

Reaktivität

  • 20
  • 17
  • 3
  • 1
Human, Ratte, Maus

Wirt

  • 32
  • 3
Kaninchen

Klonalität

  • 33
  • 2
Polyklonal

Konjugat

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ATP13A2 Antikörper ist konjugiert mit PE

Applikation

Bitte anfragen
  • Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human ATP13A2

    Isotyp

    IgG
  • Kommentare

    Exitation/Emission: 480,565nm/578nm

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at 4°C

    Haltbarkeit

    12 months
  • Target

    ATP13A2 (ATPase Type 13A2 (ATP13A2))

    Andere Bezeichnung

    Park9/Atp13a2

    Hintergrund

    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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