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MROH9 anticorps (AbBy Fluor® 350)

MROH9 Reactivité: Rat, Humain, Souris WB, IF (p) Hôte: Lapin Polyclonal AbBy Fluor® 350
N° du produit ABIN1404609
  • Antigène Tous les produits MROH9
    MROH9 (Maestro Heat-Like Repeat Family Member 9 (MROH9))
    Reactivité
    Rat, Humain, Souris
    Hôte
    • 29
    Lapin
    Clonalité
    • 29
    Polyclonal
    Conjugué
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp MROH9 est conjugé à/à la AbBy Fluor® 350
    Application
    • 29
    • 25
    • 13
    • 6
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C1orf129
    Isotype
    IgG
  • Indications d'application
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Date de péremption
    12 months
  • Antigène
    MROH9 (Maestro Heat-Like Repeat Family Member 9 (MROH9))
    Autre désignation
    C1orf129 (MROH9 Produits)
    Synonymes
    anticorps C1orf129, anticorps ARMC11, anticorps maestro heat like repeat family member 9, anticorps MROH9
    Sujet

    Synonyms: Armadillo repeat containing 11, ARMC11, C1orf129, CA129_HUMAN, Chromosome 1 open reading frame 129, FLJ23550, RP5-1092L12.1, Uncharacterized protein C1orf129.

    Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf129 gene product has been provisionally designated C1orf129 pending further characterization.

    ID gène
    80133
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