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CXX1 antibody (Biotin)

FAM127A Reactivity: Human, Mouse, Rat WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1403389
  • Target See all CXX1 (FAM127A) Antibodies
    CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
    Reactivity
    Human, Mouse, Rat
    Host
    • 35
    • 2
    Rabbit
    Clonality
    • 37
    Polyclonal
    Conjugate
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This CXX1 antibody is conjugated to Biotin
    Application
    • 26
    • 19
    • 14
    • 13
    • 7
    • 5
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human CXX1/Cerebral protein 5
    Isotype
    IgG
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  • Application Notes
    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.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C for 12 months.
    Expiry Date
    12 months
  • Target
    CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
    Alternative Name
    Cerebral protein 5 (FAM127A Products)
    Synonyms
    CXX1 antibody, MAR8C antibody, MART8C antibody, Mar8 antibody, Mart8 antibody, retrotransposon Gag like 8C antibody, RTL8C antibody
    Background

    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.

    Gene ID
    8933
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