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Chromosome 7 Open Reading Frame 10 (C7orf10) antibody (FITC) Primary Antibody

C7orf10 Reactivity: Human, Mouse, Rat IF (p) Host: Rabbit Polyclonal FITC
Catalog No. ABIN1710209
$442.20
Plus shipping costs $45.00
100 μL
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  • Target
    Chromosome 7 Open Reading Frame 10 (C7orf10)
    Reactivity
    Human, Mouse, Rat
    • 23
    • 17
    • 16
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Host
    Rabbit
    Clonality
    Polyclonal
    Conjugate
    FITC
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Application
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    • 12
    • 9
    • 5
    • 3
    • 1
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C7orf10
    Isotype
    IgG
  • Application Notes
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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
    4 °C
    Storage Comment
    Store at 4°C
    Expiry Date
    12 months
  • Target
    Chromosome 7 Open Reading Frame 10 (C7orf10)
    Alternative Name
    C7orf10 (C7orf10 Antibody Abstract)
    Synonyms
    DERP13, ORF19, c7orf10, sugct, succinyl-CoA:glutarate-CoA transferase, succinyl-CoA:glutarate-CoA transferase L homeolog, SUGCT, sugct.L
    Background

    Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.

    Synonyms: Chromosome 7 open reading frame 10, Dermal papilla derived protein 13, DERP13, FLJ11808, Hypothetical protein LOC79783, ORF19, Russel-Silver syndrome candidate, Uncharacterized protein C7orf10,CG010_HUMAN.

    Gene ID
    79783
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