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Ataxin 3 anticorps

Cet anticorps anti-Ataxin 3 est un anticorps Lapin Polyclonal détectant Ataxin 3 dans WB et IF. Adapté pour Humain et Souris.
N° du produit ABIN6567724

Aperçu rapide pour Ataxin 3 anticorps (ABIN6567724)

Antigène

Voir toutes Ataxin 3 (ATXN3) Anticorps
Ataxin 3 (ATXN3)

Reactivité

  • 58
  • 31
  • 30
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Souris

Hôte

  • 54
  • 2
  • 2
Lapin

Clonalité

  • 56
  • 2
Polyclonal

Conjugué

  • 26
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Ataxin 3 est non-conjugé

Application

  • 46
  • 20
  • 19
  • 13
  • 13
  • 11
  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogène

    Recombinant protein of human ATXN3

    Isotype

    IgG
  • Indications d'application

    WB 1:500 - 1:2000 IF 1:50 - 1:200

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    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

    Ataxin 3 (ATXN3)

    Autre désignation

    ATXN3

    Sujet

    Synonyms: AT3,Ataxin 3,ataxin 3 variant h,ataxin 3 variant m,ataxin 3 variant ref,Ataxin-3,ATX3,ATX3,ATXN3,EC 3.4.22.,JOS,Josephin,Machado Joseph disease (spinocerebellar ataxia 3,olivopontocerebellar ataxia 3,autosomal dominant,ataxin 3),Machado Joseph disease,Machado Joseph disease protein 1,Machado-Joseph disease protein 1,Machado-Joseph disease protein 1 homolog,MJD,MJD gene,MJD1,Olivopontocerebellar ataxia 3,OTTHUMP00000221583,OTTHUMP00000221585,OTTHUMP00000221586,OTTHUMP00000221587,OTTHUMP00000231995,OTTHUMP00000231997,Rsca3,SCA3,SCA3 gene,Spinocerebellar ataxia type 3 protein

    Background: Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by this gene contains (CAG)n repeats in the coding region, and the expansion of these repeats from the normal 12-44 to 52-86 is one cause of Machado-Joseph disease. There is a negative correlation between the age of onset and CAG repeat numbers. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

    Poids moléculaire

    Observed_MW: 50kDa

    Calculated_MW: 20kDa/35kDa/39kDa/41kDa

    ID gène

    4287

    UniProt

    P54252
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