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C1orf101 anticorps

C1ORF101 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246079
  • Antigène Tous les produits C1orf101 (C1ORF101)
    C1orf101 (C1ORF101) (Chromosome 1 Open Reading Frame 101 (C1ORF101))
    Reactivité
    • 12
    • 1
    Humain
    Hôte
    • 12
    Lapin
    Clonalité
    • 12
    Polyclonal
    Conjugué
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C1orf101 est non-conjugé
    Application
    • 4
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human C1orf101
    Isotype
    IgG
  • Indications d'application
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.1 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    C1orf101 (C1ORF101) (Chromosome 1 Open Reading Frame 101 (C1ORF101))
    Autre désignation
    C1orf101 (C1ORF101 Produits)
    Synonymes
    anticorps RP11-523K4.1, anticorps catsper channel auxiliary subunit epsilon, anticorps CATSPERE
    Sujet
    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 C1orf101 gene product has been provisionally designated C1orf101 pending further characterization.
    UniProt
    Q5SY80
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