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CXX1 anticorps (Biotin)

FAM127A Reactivité: Humain, Souris, Rat WB, IHC (p) Hôte: Lapin Polyclonal Biotin
N° du produit ABIN1403389
  • Antigène Voir toutes CXX1 (FAM127A) Anticorps
    CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 35
    • 2
    Lapin
    Clonalité
    • 37
    Polyclonal
    Conjugué
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp CXX1 est conjugé à/à la Biotin
    Application
    • 26
    • 19
    • 14
    • 13
    • 7
    • 5
    • 3
    • 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 CXX1/Cerebral protein 5
    Isotype
    IgG
    Top Product
    Discover our top product FAM127A Anticorps primaire
  • 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
    CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
    Autre désignation
    Cerebral protein 5 (FAM127A Produits)
    Synonymes
    anticorps CXX1, anticorps MAR8C, anticorps MART8C, anticorps Mar8, anticorps Mart8, anticorps retrotransposon Gag like 8C, anticorps RTL8C
    Sujet

    Synonyms: Mammalian retrotransposon derived protein 8C, CAAX box protein 1, Cerebral protein 5, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mar8, MAR8C, Mart8, F127A_HUMAN.

    Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.

    ID gène
    8933
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