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C9orf41 Antikörper (AA 101-200) (Biotin)

Dieser Anti-C9orf41 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von C9orf41 in ELISA, IHC (p) und IHC (fro). Geeignet für Ratte und Maus.
Produktnummer ABIN1700796

Kurzübersicht für C9orf41 Antikörper (AA 101-200) (Biotin) (ABIN1700796)

Target

C9orf41 (Chromosome 9 Open Reading Frame 41 (C9orf41))

Reaktivität

  • 16
  • 15
  • 8
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Ratte, Maus

Wirt

  • 17
  • 5
Kaninchen

Klonalität

  • 17
  • 5
Polyklonal

Konjugat

  • 9
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser C9orf41 Antikörper ist konjugiert mit Biotin

Applikation

  • 13
  • 13
  • 7
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Bindungsspezifität

    • 14
    • 1
    • 1
    AA 101-200

    Kreuzreaktivität

    Maus, Ratte

    Homologie

    Human,Cow,Sheep,Pig,Chicken,Rabbit

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C9orf41

    Isotyp

    IgG
  • Applikationshinweise

    IHC-P 1:200-400
    IHC-F 1:100-500

    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

    C9orf41 (Chromosome 9 Open Reading Frame 41 (C9orf41))

    Andere Bezeichnung

    C9orf41

    Hintergrund

    Synonyms: C9orf41, CI041_HUMAN, FLJ25795, UPF0586 protein C9orf41.

    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 C9orf41 gene product has been provisionally designated C9orf41 pending further characterization.

    Gen-ID

    138199
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