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TSPY-Like 6 Antikörper

TSPYL6 Reaktivität: Human IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7192947
  • Target Alle TSPY-Like 6 (TSPYL6) Produkte
    TSPY-Like 6 (TSPYL6)
    Reaktivität
    • 26
    • 2
    • 1
    Human
    Wirt
    • 25
    • 1
    Kaninchen
    Klonalität
    • 26
    Polyklonal
    Konjugat
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TSPY-Like 6 Antikörper ist unkonjugiert
    Applikation
    • 19
    • 14
    • 13
    • 12
    • 12
    • 5
    • 2
    • 1
    Immunohistochemistry (IHC), ELISA
    Kreuzreaktivität
    Human
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human TSPYL6
    Isotyp
    IgG
  • Applikationshinweise
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Informationen zur Lagerung
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    TSPY-Like 6 (TSPYL6)
    Andere Bezeichnung
    TSPYL6 (TSPYL6 Produkte)
    Synonyme
    TSPY like 6 antikoerper, TSPYL6 antikoerper
    Hintergrund

    Background: TSPYL6 (Testis-specific Y-encoded-like protein 6) is a 410 amino acid member of the nucleosome assembly protein (NAP) family. TSPYL6 is believed to be similar to Testis-specific Y-encoded protein 1 in form and function. The gene that encodes TSPYL6 is found on chromosome 2 which consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr m syndrome is due to mutations in the ALMS1 gene.

    Aliases: TSPY-like 6

    UniProt
    Q8N831
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