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SPG7 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement SPG7 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN5515659

Aperçu rapide pour SPG7 anticorps (N-Term) (ABIN5515659)

Antigène

Voir toutes SPG7 Anticorps
SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivité

  • 25
  • 5
  • 3
  • 3
  • 1
  • 1
Humain

Hôte

  • 18
  • 10
Lapin

Clonalité

  • 20
  • 8
Polyclonal

Conjugué

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SPG7 est non-conjugé

Application

  • 26
  • 11
  • 10
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Séquence

    LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE

    Purification

    Affinity purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the N terminal region of human SPG7
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    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.
  • Antigène

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Autre désignation

    SPG7

    Sujet

    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

    ID gène

    6687

    NCBI Accession

    NM_003119, NP_003110
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