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ST7 Antikörper (AA 268-309)

ST7 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5708171
  • Target Alle ST7 Antikörper anzeigen
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Bindungsspezifität
    • 9
    • 7
    • 7
    • 6
    • 2
    • 1
    • 1
    AA 268-309
    Reaktivität
    • 21
    • 3
    • 3
    Human
    Wirt
    • 21
    • 1
    Kaninchen
    Klonalität
    • 22
    Polyklonal
    Konjugat
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser ST7 Antikörper ist unkonjugiert
    Applikation
    • 21
    • 16
    • 14
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Aufreinigung
    Antigen affinity purified
    Immunogen
    Amino acids 268-309 (DGCYRRSQQLQHHGSQYEAQHRRDTNVLVYIKRRLAMCARRL-human) were used as the immunogen for the ST7 antibody.
    Isotyp
    IgG
    Top Product
    Discover our top product ST7 Primärantikörper
  • Applikationshinweise
    Optimal dilution of the ST7 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Lagerung
    -20 °C
    Informationen zur Lagerung
    After reconstitution, the ST7 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Andere Bezeichnung
    Suppressor of Tumorigenicity 7 (ST7 Produkte)
    Synonyme
    ETS7q antikoerper, FAM4A antikoerper, FAM4A1 antikoerper, HELG antikoerper, RAY1 antikoerper, SEN4 antikoerper, TSG7 antikoerper, 9430001H04Rik antikoerper, Fam4a2 antikoerper, suppression of tumorigenicity 7 antikoerper, ST7 antikoerper, St7 antikoerper
    Hintergrund
    Suppressor of tumorigenicity protein 7 is a protein that in humans is encoded by the ST7 gene. The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described.
    UniProt
    Q9NRC1
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