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C2orf57 anticorps (Cy3)

C2orf57 Reactivité: Humain WB, IF (p) Hôte: Lapin Polyclonal Cy3
N° du produit ABIN1422713
  • Antigène Tous les produits C2orf57
    C2orf57 (Chromosome 2 Open Reading Frame 57 (C2orf57))
    Reactivité
    Humain
    Hôte
    • 14
    • 1
    Lapin
    Clonalité
    • 15
    Polyclonal
    Conjugué
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C2orf57 est conjugé à/à la Cy3
    Application
    • 15
    • 12
    • 3
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
     Réactivité croisée
    Humain
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C2orf57
    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
    C2orf57 (Chromosome 2 Open Reading Frame 57 (C2orf57))
    Autre désignation
    C2orf57 (C2orf57 Produits)
    Synonymes
    anticorps testis expressed 44, anticorps TEX44
    Sujet

    Synonyms: Chromosome 2 open reading frame 57, Hypothetical protein LOC165100, MGC35154, Uncharacterized protein C2orf57, CB057_HUMAN.

    Background: C2orf57, also known as MGC35154, is a 395 amino acid protein encoded by a gene that maps to human chromosome 2q37.1. 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.

    ID gène
    165100
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