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C21ORF56 anticorps (Biotin)

C21orf56 Reactivité: Humain, Souris, Rat WB, IHC (p) Hôte: Lapin Polyclonal Biotin
N° du produit ABIN1405717
  • Antigène Tous les produits C21ORF56 (C21orf56)
    C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
    Reactivité
    • 38
    • 18
    • 18
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 37
    • 1
    Lapin
    Clonalité
    • 37
    • 1
    Polyclonal
    Conjugué
    • 11
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C21ORF56 est conjugé à/à la Biotin
    Application
    • 33
    • 17
    • 13
    • 3
    • 2
    • 1
    • 1
    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 C21ORF56
    Isotype
    IgG
  • 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
    C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
    Autre désignation
    C21ORF56 (C21orf56 Produits)
    Synonymes
    anticorps C21orf56, anticorps spermatogenesis and centriole associated 1 like, anticorps SPATC1L
    Sujet

    Synonyms: Chromosome 21 open reading frame 56, DKFZp434N0650, MGC99490, Uncharacterized protein C21orf56, SPC1L_HUMAN.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterization.

    ID gène
    84221
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