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C2orf55 anticorps (Cy5)

C2orf55 Reactivité: Humain, Rat, Souris WB, IF (p) Hôte: Lapin Polyclonal Cy5
N° du produit ABIN1422708
  • Antigène Tous les produits C2orf55
    C2orf55 (Chromosome 2 Open Reading Frame 55 (C2orf55))
    Reactivité
    • 17
    • 15
    • 14
    • 2
    • 2
    • 1
    Humain, Rat, Souris
    Hôte
    • 17
    Lapin
    Clonalité
    • 17
    Polyclonal
    Conjugué
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C2orf55 est conjugé à/à la Cy5
    Application
    • 17
    • 12
    • 3
    • 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 C2orf55
    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
    C2orf55 (Chromosome 2 Open Reading Frame 55 (C2orf55))
    Autre désignation
    C2orf55 (C2orf55 Produits)
    Synonymes
    anticorps C2orf55, anticorps KIAA1211 like, anticorps KIAA1211L
    Sujet

    Synonyms: Chromosome 2 open reading frame 55, Hypothetical protein LOC343990, K121L_HUMAN.

    Background: C2orf55, also known as MGC42367, is a 962 amino acid protein that is encoded by a gene located on human chromosome 2q11.2. The second largest human chromosome, chromosome 2 consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid 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 due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

    ID gène
    343990
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