Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

SPG7 Antikörper (N-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SPG7 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN5515659

Kurzübersicht für SPG7 Antikörper (N-Term) (ABIN5515659)

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
    N-Term

    Sequenz

    LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE

    Aufreinigung

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human SPG7
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Andere Bezeichnung

    SPG7

    Hintergrund

    This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA 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. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.

    Alias Symbols: CAR, PGN, CMAR, SPG5C

    Protein Size: 489

    Gen-ID

    6687

    NCBI Accession

    NM_003119, NP_003110
Sie sind hier:
Chat with us!