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C7ORF57 Antikörper (AA 161-260) (Biotin)

C7ORF57 Reaktivität: Ratte IHC (fro), IHC (p), ELISA Wirt: Kaninchen Polyclonal Biotin
Produktnummer ABIN1700845
  • Target Alle C7ORF57 Produkte
    C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
    Bindungsspezifität
    • 14
    • 1
    • 1
    AA 161-260
    Reaktivität
    • 16
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Ratte
    Wirt
    • 16
    Kaninchen
    Klonalität
    • 16
    Polyklonal
    Konjugat
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C7ORF57 Antikörper ist konjugiert mit Biotin
    Applikation
    • 13
    • 13
    • 2
    • 2
    • 2
    • 2
    • 1
    Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
    Kreuzreaktivität
    Ratte
    Homologie
    Human,Mouse,Cow,Sheep,Horse
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C7orf57
    Isotyp
    IgG
  • Applikationshinweise
    IHC-P 1:200-400
    IHC-F 1:100-500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C for 12 months.
    Haltbarkeit
    12 months
  • Target
    C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
    Andere Bezeichnung
    C7orf57 (C7ORF57 Produkte)
    Synonyme
    C7orf57 antikoerper, chromosome 4 open reading frame, human C7orf57 antikoerper, chromosome 7 open reading frame 57 antikoerper, C4H7orf57 antikoerper, C7orf57 antikoerper
    Hintergrund

    Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.

    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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.

    Gen-ID
    136288
    UniProt
    Q8NEG2
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