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FAM107A antibody

FAM107A Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7236939
  • Target See all FAM107A Antibodies
    FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
    Reactivity
    • 24
    • 10
    • 7
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 20
    • 4
    Rabbit
    Clonality
    • 22
    • 2
    Polyclonal
    Conjugate
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM107A antibody is un-conjugated
    Application
    • 10
    • 7
    • 5
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human FAM107A
    Isotype
    IgG
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.7 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
    Alternative Name
    FAM107A (FAM107A Products)
    Synonyms
    drr1 antibody, tu3a antibody, xdrr1 antibody, DRR1 antibody, TU3A antibody, Drr1 antibody, RGD1306327 antibody, Tu3a antibody, family with sequence similarity 107 member A S homeolog antibody, family with sequence similarity 107 member A antibody, family with sequence similarity 107, member A antibody, fam107a.S antibody, FAM107A antibody, Fam107a antibody
    Background
    FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
    UniProt
    O95990
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