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SPG7 Antikörper (AA 384-568)

Der Kaninchen Polyklonal Anti-SPG7-Antikörper wurde für WB validiert. Er ist geeignet, SPG7 in Proben von Human zu detektieren.
Produktnummer ABIN1886423

Kurzübersicht für SPG7 Antikörper (AA 384-568) (ABIN1886423)

Target

Alle SPG7 Antikörper anzeigen
SPG7 (Spastic Paraplegia 7 (SPG7))

Reaktivität

  • 23
  • 3
  • 3
  • 2
  • 1
  • 1
Human

Wirt

  • 16
  • 10
Kaninchen

Klonalität

  • 18
  • 8
Polyklonal

Konjugat

  • 21
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SPG7 Antikörper ist unkonjugiert

Applikation

  • 24
  • 11
  • 10
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 384-568

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 384 and 568 of SPG7
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Andere Bezeichnung

    SPG7

    Hintergrund

    This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family.Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis.Two transcript variants encoding distinct isoforms have been identified for this gene.Mutations associated with this gene cause autosomal recessive spastic paraplegia 7.[provided by RefSeq]

    Molekulargewicht

    88 kDa

    Gen-ID

    6687
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