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SPG7 anticorps (AA 1-250)

Cet anticorps anti-SPG7 est un anticorps Lapin Polyclonal détectant SPG7 dans WB et IHC. Adapté pour Humain.
N° du produit ABIN6148342

Aperçu rapide pour SPG7 anticorps (AA 1-250) (ABIN6148342)

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
  • 10
  • 10
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-250

    Séquence

    MAVLLLLLRA LRRGPGPGPR PLWGPGPAWS PGFPARPGRG RPYMASRPPG DLAEAGGRAL QSLQLRLLTP TFEGINGLLL KQHLVQNPVR LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE RLRTLLVIAV VMSLLNALST SGGSISWNDF VHEMLAKGEV QRVQVVPESD VVEVYLHPGA VVFGRPRLAL MYRMQVANID KFEEKLRAAE DELNIEAKDR IPVSYKRTGF

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human SPG7 (NP_003110.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:1000 - 1:2000,IHC,1:50 - 1:200

    Commentaires

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid 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.,SPG7,CAR,CMAR,PGN,SPG5C,Cell Biology & Developmental Biology,Ubiquitin,Neuroscience,Neurodegenerative Diseases,SPG7

    Poids moléculaire

    53 kDa/88 kDa

    ID gène

    6687

    UniProt

    Q9UQ90
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