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C12orf53 anticorps (Biotin)

C12orf53 Reactivité: Humain, Souris, Rat WB, IHC (p) Hôte: Lapin Polyclonal Biotin
N° du produit ABIN1405633
  • Antigène Voir toutes C12orf53 Anticorps
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Reactivité
    • 35
    • 29
    • 21
    • 6
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    Humain, Souris, Rat
    Hôte
    • 35
    Lapin
    Clonalité
    • 35
    Polyclonal
    Conjugué
    • 8
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C12orf53 est conjugé à/à la Biotin
    Application
    • 34
    • 13
    • 13
    • 13
    • 13
    • 4
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C12ORF53
    Isotype
    IgG
    Top Product
    Discover our top product C12orf53 Anticorps primaire
  • Indications d'application
    WB 1:300-5000
    IHC-P 1:200-400
    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
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Autre désignation
    C12ORF53 (C12orf53 Produits)
    Synonymes
    anticorps C12orf53, anticorps PANP, anticorps leda-1, anticorps PILR alpha associated neural protein, anticorps PIANP
    Sujet

    Synonyms: Chromosome 12 open reading frame 53, DKFZp547D2210, Hypothetical protein LOC196500, Uncharacterized protein C12orf53, PIANP_HUMAN.

    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 C12orf53 gene product has been provisionally designated C12orf53 pending further characterization.

    ID gène
    196500
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