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FAM96B Antikörper (Cy3)

FAM96B Reaktivität: Human, Maus, Ratte WB, IF (p) Wirt: Kaninchen Polyclonal Cy3
Produktnummer ABIN1422191
  • Target Alle FAM96B Antikörper anzeigen
    FAM96B (Family with Sequence Similarity 96, Member B (FAM96B))
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 38
    Kaninchen
    Klonalität
    • 38
    Polyklonal
    Konjugat
    • 14
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser FAM96B Antikörper ist konjugiert mit Cy3
    Applikation
    • 37
    • 17
    • 15
    • 14
    • 12
    • 6
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human FAM96B
    Isotyp
    IgG
    Top Product
    Discover our top product FAM96B Primärantikörper
  • Applikationshinweise
    IF(IHC-P) 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
    FAM96B (Family with Sequence Similarity 96, Member B (FAM96B))
    Andere Bezeichnung
    FAM96B (FAM96B Produkte)
    Synonyme
    MIP18 antikoerper, 1110019N10Rik antikoerper, RGD1311762 antikoerper, family with sequence similarity 96 member B antikoerper, family with sequence similarity 96, member B antikoerper, FAM96B antikoerper, Fam96b antikoerper
    Hintergrund

    Synonyms: Mitotic spindle-associated MMXD complex subunit MIP18, MSS19-interacting protein of 18 kDa, Protein FAM96B, MIP18_HUMAN.

    Background: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM96B gene product has been provisionally designated FAM96B pending further characterization.

    Gen-ID
    51647
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