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FAM207A anticorps (AA 95-120)

FAM207A Reactivité: Humain IF (p), IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1385685
  • Antigène Tous les produits FAM207A
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    Épitope
    • 14
    • 7
    • 1
    AA 95-120
    Reactivité
    • 22
    • 8
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 22
    Lapin
    Clonalité
    • 22
    Polyclonal
    Conjugué
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FAM207A est non-conjugé
    Application
    • 12
    • 8
    • 7
    • 6
    • 3
    Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Humain
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C21orf70
    Isotype
    IgG
  • Indications d'application
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    Autre désignation
    C21orf70 (FAM207A Produits)
    Synonymes
    anticorps C21orf70, anticorps 1810008A18Rik, anticorps AI303072, anticorps family with sequence similarity 207 member A, anticorps family with sequence similarity 207, member A, anticorps FAM207A, anticorps Fam207a
    Sujet

    Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.

    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 C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

    ID gène
    85395
    UniProt
    Q9NSI2
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