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C9ORF72 Antikörper (AA 391-481) (PE)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch C9ORF72 in WB und FACS. Er zeigt eine Reaktivität gegenüber Human, Ratte und Maus.
Produktnummer ABIN7090986

Kurzübersicht für C9ORF72 Antikörper (AA 391-481) (PE) (ABIN7090986)

Target

Alle C9ORF72 Antikörper anzeigen
C9ORF72 (Chromosome 9 Open Reading Frame 72 (C9ORF72))

Reaktivität

  • 44
  • 25
  • 22
  • 1
Human, Ratte, Maus

Wirt

  • 37
  • 5
  • 2
Kaninchen

Klonalität

  • 40
  • 4
Polyklonal

Konjugat

  • 19
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser C9ORF72 Antikörper ist konjugiert mit PE

Applikation

  • 36
  • 25
  • 18
  • 13
  • 13
  • 8
  • 7
  • 6
  • 5
  • 5
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 8
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 391-481

    Kreuzreaktivität

    Human, Maus, Ratte

    Homologie

    Dog,Cow,Pig,Horse,Chicken

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C9orf72

    Isotyp

    IgG
  • Applikationshinweise

    FCM 1:20-100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Target

    C9ORF72 (Chromosome 9 Open Reading Frame 72 (C9ORF72))

    Andere Bezeichnung

    C9orf72

    Hintergrund

    Synonyms: ALSFTD, FTDALS, Protein C9orf72, C9orf72

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf72 gene product has been provisionally designated C9orf72 pending further characterization. There are two isoforms of C9orf72 that are produced as a result of alternative splicing events.

    Gen-ID

    203228

    UniProt

    Q96LT7
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