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C9orf68 anticorps (AA 201-300) (Biotin)

C9orf68 Reactivité: Humain IHC (fro), IHC (p), ELISA Hôte: Lapin Polyclonal Biotin
N° du produit ABIN1699952
  • Antigène Tous les produits C9orf68
    C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
    Épitope
    • 14
    • 1
    • 1
    • 1
    AA 201-300
    Reactivité
    Humain
    Hôte
    • 16
    • 2
    Lapin
    Clonalité
    • 18
    Polyclonal
    Conjugué
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C9orf68 est conjugé à/à la Biotin
    Application
    • 13
    • 13
    • 4
    • 2
    • 2
    • 2
    • 1
    Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
    Homologie
    Human
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C9orf68
    Isotype
    IgG
  • Indications d'application
    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.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C for 12 months.
    Date de péremption
    12 months
  • Antigène
    C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
    Autre désignation
    C9orf68 (C9orf68 Produits)
    Synonymes
    anticorps MGC131199, anticorps MGC146453, anticorps C9orf68, anticorps bA6J24.2, anticorps spermatogenesis associated 6-like L homeolog, anticorps spermatogenesis associated 6-like, anticorps spermatogenesis associated 6 like, anticorps spata6l.L, anticorps spata6l, anticorps SPATA6L
    Sujet

    Synonyms: bA6J24.2, chromosome 9 open reading frame 68, FLJ10058, RP11-280I16.2, Uncharacterized protein C9orf68,SPA6L_HUMAN.

    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 C9orf68 gene product has been provisionally designated C9orf68 pending further characterization. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.

    ID gène
    55064
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