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ST7 Antikörper (AA 169-197)

Dieses Anti-ST7-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von ST7 in WB und FACS. Geeignet für Human.
Produktnummer ABIN5532994

Kurzübersicht für ST7 Antikörper (AA 169-197) (ABIN5532994)

Target

Alle ST7 Antikörper anzeigen
ST7 (Suppression of Tumorigenicity 7 (ST7))

Reaktivität

  • 16
  • 4
  • 4
Human

Wirt

  • 16
  • 1
Kaninchen

Klonalität

  • 17
Polyklonal

Konjugat

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
Dieser ST7 Antikörper ist unkonjugiert

Applikation

  • 16
  • 12
  • 11
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 8
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    AA 169-197

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This ST7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 169-197 amino acids from the Central region of human ST7.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    For WB starting dilution is: 1:1000

    For FACS starting dilution is: 1:10~50

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    ST7 (Suppression of Tumorigenicity 7 (ST7))

    Andere Bezeichnung

    ST7

    Hintergrund

    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.

    Molekulargewicht

    67 kDa

    Gen-ID

    7982

    UniProt

    Q9NRC1
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