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MROH9 antibody (Biotin)

MROH9 Reactivity: Rat, Human, Mouse WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1404613
  • Target See all MROH9 products
    MROH9 (Maestro Heat-Like Repeat Family Member 9 (MROH9))
    Reactivity
    Rat, Human, Mouse
    Host
    • 29
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This MROH9 antibody is conjugated to Biotin
    Application
    • 29
    • 26
    • 13
    • 5
    • 3
    • 3
    • 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 C1orf129
    Isotype
    IgG
  • 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
    MROH9 (Maestro Heat-Like Repeat Family Member 9 (MROH9))
    Alternative Name
    C1orf129 (MROH9 Products)
    Synonyms
    C1orf129 antibody, ARMC11 antibody, maestro heat like repeat family member 9 antibody, MROH9 antibody
    Background

    Synonyms: Armadillo repeat containing 11, ARMC11, C1orf129, CA129_HUMAN, Chromosome 1 open reading frame 129, FLJ23550, RP5-1092L12.1, Uncharacterized protein C1orf129.

    Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf129 gene product has been provisionally designated C1orf129 pending further characterization.

    Gene ID
    80133
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