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C9orf152 Antikörper

C9orf152 Reaktivität: Human, Maus, Ratte WB, IF (p), IHC (p) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1385420
  • Target Alle C9orf152 Produkte
    C9orf152 (Chromosome 9 Open Reading Frame 152 (C9orf152))
    Reaktivität
    • 18
    • 15
    • 14
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 16
    • 2
    Kaninchen
    Klonalität
    • 18
    Polyklonal
    Konjugat
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C9orf152 Antikörper ist unkonjugiert
    Applikation
    • 18
    • 12
    • 2
    • 2
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C9orf152
    Isotyp
    IgG
  • Applikationshinweise
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    Informationen zur Lagerung
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Haltbarkeit
    12 months
  • Target
    C9orf152 (Chromosome 9 Open Reading Frame 152 (C9orf152))
    Andere Bezeichnung
    C9orf152 (C9orf152 Produkte)
    Synonyme
    bA470J20.2 antikoerper, chromosome 9 open reading frame 152 antikoerper, chromosome 15 open reading frame, human C9orf152 antikoerper, C9orf152 antikoerper, C15H9orf152 antikoerper
    Hintergrund

    Synonyms: Chromosome 9 open reading frame 152, Hypothetical protein LOC401546, Uncharacterized protein C9orf152, CI152_HUMAN.

    Background: C9orf152 is a 239 amino acid protein encoded by a gene that maps to human chromosome 9q31.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.

    Gen-ID
    401546
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