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Sacsin anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement Sacsin dans WB. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN5673657
534,11 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 6 à 8 jours ouvrables

Aperçu rapide pour Sacsin anticorps (C-Term) (ABIN5673657)

Antigène

Voir toutes Sacsin (SACS) Anticorps
Sacsin (SACS) (Spastic Ataxia of Charlevoix-Saguenay (Sacsin) (SACS))

Reactivité

  • 11
  • 5
  • 1
Humain

Hôte

  • 10
  • 1
Lapin

Clonalité

  • 11
Polyclonal

Conjugué

  • 7
  • 2
  • 1
  • 1
Cet anticorp Sacsin est non-conjugé

Application

  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 5
    • 2
    • 1
    • 1
    • 1
    C-Term

    Séquence

    VVEQAWKLPE SERKKIIRRL YLKWHPDKNP ENHDIANEVF KHLQNEINRL

    Purification

    Affinity purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the C terminal region of human SACS
  • 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

    Sacsin (SACS) (Spastic Ataxia of Charlevoix-Saguenay (Sacsin) (SACS))

    Autre désignation

    SACS

    Sujet

    This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. The authors of a publication on the effects of siRNA-mediated sacsin knockdown concluded that sacsin protects against mutant ataxin-1 and suggest that "the large multi-domain sacsin protein is able to recruit Hsp70 chaperone action and has the potential to regulate the effects of other ataxia proteins". A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants.

    Alias Symbols: SPAX6, ARSACS, DNAJC29, PPP1R138

    Protein Size: 309

    ID gène

    26278

    NCBI Accession

    NM_014363, NP_055178

    UniProt

    Q7Z6W7
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