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C8orf47 antibody (AA 1-100)

C8ORF47 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1713442
  • Target See all C8orf47 (C8ORF47) products
    C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
    Binding Specificity
    AA 1-100
    Reactivity
    Human
    Host
    • 14
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C8orf47 antibody is un-conjugated
    Application
    Western Blotting (WB)
    Cross-Reactivity
    Human
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C8orf47
    Isotype
    IgG
  • Application Notes
    WB 1:300-5000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    Storage Comment
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Expiry Date
    12 months
  • Target
    C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
    Alternative Name
    C8orf47 (C8ORF47 Products)
    Synonyms
    glutamate rich 5 antibody, ERICH5 antibody
    Background

    Synonyms: C8orf47, CH047_HUMAN, Chromosome 8 open reading frame 47, Uncharacterized protein C8orf47.

    Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.

    Gene ID
    203111
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