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C12ORF54 anticorps (Cy3)

C12ORF54 Reactivité: Humain, Souris, Rat WB, IF (p) Hôte: Lapin Polyclonal Cy3
N° du produit ABIN1423505
  • Antigène Tous les produits C12ORF54
    C12ORF54 (Chromosome 12 Open Reading Frame 54 (C12ORF54))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 16
    Lapin
    Clonalité
    • 16
    Polyclonal
    Conjugué
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C12ORF54 est conjugé à/à la Cy3
    Application
    • 15
    • 12
    • 3
    • 1
    • 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 C12ORF54
    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
    C12ORF54 (Chromosome 12 Open Reading Frame 54 (C12ORF54))
    Autre désignation
    C12ORF54 (C12ORF54 Produits)
    Synonymes
    anticorps HSD-29, anticorps HSD-30, anticorps chromosome 12 open reading frame 54, anticorps C12orf54
    Sujet

    Synonyms: MGC35033, C12orf54, Chromosome 12 open reading frame 54, CL054_HUMAN, HSD 29, HSD 30, HSD29, Uncharacterized protein C12orf54.

    Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf54 gene product has been provisionally designated C12orf54 pending further characterization.

    ID gène
    121273
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