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C9ORF50 anticorps (AA 31-130) (HRP)

C9ORF50 Reactivité: Humain IHC (p), IHC (fro), WB Hôte: Lapin Polyclonal HRP
N° du produit ABIN1710965
  • Antigène Tous les produits C9ORF50
    C9ORF50 (Chromosome 9 Open Reading Frame 50 (C9ORF50))
    Épitope
    AA 31-130
    Reactivité
    Humain
    Hôte
    • 14
    Lapin
    Clonalité
    • 14
    Polyclonal
    Conjugué
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C9ORF50 est conjugé à/à la HRP
    Application
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Western Blotting (WB)
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C9orf50
    Isotype
    IgG
  • Indications d'application
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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.
    Conseil sur la manipulation
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    Stock
    -20 °C/-80 °C
    Stockage commentaire
    Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles
    Date de péremption
    12 months
  • Antigène
    C9ORF50 (Chromosome 9 Open Reading Frame 50 (C9ORF50))
    Autre désignation
    C9orf50 (C9ORF50 Produits)
    Synonymes
    anticorps chromosome 9 open reading frame 50, anticorps C9orf50
    Sujet

    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 C9orf50 gene product has been provisionally designated C9orf50 pending further characterization.

    Subcellular location: Nucleus

    Synonyms: C9orf50, CI050_HUMAN, Uncharacterized protein C9orf50.

    ID gène
    375759
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