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FAM107A antibody (Family with Sequence Similarity 107, Member A) Primary Antibody

FAM107A Reactivity: Human, Mouse, Rat IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2423423
$493.90
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  • Target
    FAM107A
    Reactivity
    Human, Mouse, Rat
    • 21
    • 7
    • 6
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Host
    Rabbit
    • 19
    • 2
    Clonality
    Polyclonal
    • 21
    Conjugate
    This FAM107A antibody is un-conjugated
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Application
    Immunohistochemistry (IHC), ELISA
    • 10
    • 8
    • 5
    • 3
    • 1
    Purification
    Antigen affinity purification
    Immunogen
    Recombinant protein of human FAM107A
    Isotype
    IgG
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C/-80 °C
    Storage Comment
    Store at -20°C (regular) and -80°C (long term).
  • Target
    FAM107A
    Alternative Name
    FAM107A (FAM107A Antibody Abstract)
    Synonyms
    drr1, tu3a, xdrr1, DRR1, TU3A, Drr1, RGD1306327, Tu3a, family with sequence similarity 107 member A S homeolog, family with sequence similarity 107 member A, family with sequence similarity 107, member A, fam107a.S, FAM107A, Fam107a
    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.
    Synonyms: DRR1, TU3A
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