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BUD31 anticorps

L’anticorps Lapin Polyclonal anti-BUD31 a été validé pour WB, ELISA et IHC. Il convient pour détecter BUD31 dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN7246052

Aperçu rapide pour BUD31 anticorps (ABIN7246052)

Antigène

Voir toutes BUD31 Anticorps
BUD31 (BUD31 Homolog (BUD31))

Reactivité

  • 45
  • 29
  • 21
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 41
  • 4
Lapin

Clonalité

  • 42
  • 3
Polyclonal

Conjugué

  • 27
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp BUD31 est non-conjugé

Application

  • 24
  • 16
  • 10
  • 6
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Full length fusion protein

    Isotype

    IgG
  • Indications d'application

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.5 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    BUD31 (BUD31 Homolog (BUD31))

    Autre désignation

    BUD31

    Sujet

    BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 17 kDa

    UniProt

    P41223
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