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HBa2 Antikörper

HBa2 Reaktivität: Maus, Ratte IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7264463
  • Target Alle HBa2 Antikörper anzeigen
    HBa2 (Hemoglobin, alpha 2 (HBa2))
    Reaktivität
    • 8
    • 3
    • 1
    Maus, Ratte
    Wirt
    • 9
    Kaninchen
    Klonalität
    • 9
    Polyklonal
    Konjugat
    • 5
    • 1
    • 1
    • 1
    • 1
    Dieser HBa2 Antikörper ist unkonjugiert
    Applikation
    • 9
    • 6
    • 5
    • 5
    • 1
    • 1
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human HBA2 (NP_000508.1).
    Isotyp
    IgG
    Top Product
    Discover our top product HBa2 Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    HBa2 (Hemoglobin, alpha 2 (HBa2))
    Andere Bezeichnung
    HBA2 (HBa2 Produkte)
    Hintergrund
    The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97 % of the total hemoglobin, alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3 % of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1, some nondeletion alpha thalassemias have also been reported.
    Gen-ID
    3040
    UniProt
    P69905
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