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C2ORF16 anticorps (AA 1901-1984) (HRP)

C2ORF16 Reactivité: Humain IHC (fro), IHC (p) Hôte: Lapin Polyclonal HRP
N° du produit ABIN1710920
  • Antigène Tous les produits C2ORF16
    C2ORF16 (Chromosome 2 Open Reading Frame 16 (C2ORF16))
    Épitope
    AA 1901-1984
    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 C2ORF16 est conjugé à/à la HRP
    Application
    • 13
    • 13
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C2orf16
    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.
    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
    C2ORF16 (Chromosome 2 Open Reading Frame 16 (C2ORF16))
    Autre désignation
    C2orf16 (C2ORF16 Produits)
    Synonymes
    anticorps chromosome 2 open reading frame 16, anticorps C2orf16
    Sujet

    C2orf16 (chromosome 2 open reading frame 16), also known as DKFZp434G118 or DKFZp781D2023, is a 1,984 amino acid protein encoded by a gene that maps to human chromosome 2p23.3. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

    Subcellular location: Nucleus, Extracellular matrix

    Synonyms: Uncharacterized protein C2orf16, C2orf16

    ID gène
    84226
    UniProt
    Q68DN1
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