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C7orf44 Antikörper (AA 51-146) (Cy7)

C7orf44 Reaktivität: Human WB, IF (cc), IF (p) Wirt: Kaninchen Polyclonal Cy7
Produktnummer ABIN1707326
  • Target Alle C7orf44 Produkte
    C7orf44 (Chromosome 7 Open Reading Frame 44 (C7orf44))
    Bindungsspezifität
    • 14
    • 1
    AA 51-146
    Reaktivität
    Human
    Wirt
    • 14
    • 1
    Kaninchen
    Klonalität
    • 15
    Polyklonal
    Konjugat
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C7orf44 Antikörper ist konjugiert mit Cy7
    Applikation
    • 15
    • 12
    • 12
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Homologie
    Human
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C7orf44
    Isotyp
    IgG
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    C7orf44 (Chromosome 7 Open Reading Frame 44 (C7orf44))
    Andere Bezeichnung
    C7orf44 (C7orf44 Produkte)
    Synonyme
    C7orf44 antikoerper, MITRAC15 antikoerper, cytochrome c oxidase assembly factor 1 homolog antikoerper, COA1 antikoerper
    Hintergrund

    Synonyms: Chromosome 7 open reading frame 44, FLJ10803, Hypothetical protein LOC55744, Uncharacterized protein C7orf44,COA1_HUMAN.

    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 C7orf44 gene product has been provisionally designated C7orf44 pending further characterization.

    Gen-ID
    55744
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