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SPG7 anticorps (AA 384-568)

L’anticorps Lapin Polyclonal anti-SPG7 a été validé pour WB. Il convient pour détecter SPG7 dans des échantillons de Humain.
N° du produit ABIN1886423

Aperçu rapide pour SPG7 anticorps (AA 384-568) (ABIN1886423)

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
    AA 384-568

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 384 and 568 of SPG7
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Autre désignation

    SPG7

    Sujet

    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]

    Poids moléculaire

    88 kDa

    ID gène

    6687
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