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PDZD9 Antikörper (AA 50-100) (Biotin)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch PDZD9 in WB und IHC (p). Er zeigt eine Reaktivität gegenüber Human, Ratte und Maus.
Produktnummer ABIN1403767

Kurzübersicht für PDZD9 Antikörper (AA 50-100) (Biotin) (ABIN1403767)

Target

Alle PDZD9 Antikörper anzeigen
PDZD9 (PDZ Domain Containing 9 (PDZD9))

Reaktivität

  • 17
  • 15
  • 14
  • 2
  • 1
Human, Ratte, Maus

Wirt

  • 16
  • 1
Kaninchen

Klonalität

  • 17
Polyklonal

Konjugat

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser PDZD9 Antikörper ist konjugiert mit Biotin

Applikation

  • 17
  • 13
  • 2
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Bindungsspezifität

    • 14
    • 1
    • 1
    AA 50-100

    Kreuzreaktivität

    Human, Maus, Ratte

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human PDZD9

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:300-5000
    IHC-P 1:200-400

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C for 12 months.

    Haltbarkeit

    12 months
  • Target

    PDZD9 (PDZ Domain Containing 9 (PDZD9))

    Andere Bezeichnung

    PDZD9

    Hintergrund

    Synonyms: PDZ domain containing 9, PDZ domain containing protein 9, PDZD 9, PDZK-9.\, PDZD9_HUMAN.

    Background: PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.

    Gen-ID

    255762

    UniProt

    Q8IXQ8
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