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TRIP4 anticorps

Cet anticorps anti-TRIP4 est un anticorps Lapin Polyclonal détectant TRIP4 dans IHC. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7384096

Aperçu rapide pour TRIP4 anticorps (ABIN7384096)

Antigène

Voir toutes TRIP4 Anticorps
TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

Reactivité

  • 44
  • 20
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 41
  • 2
  • 1
Lapin

Clonalité

  • 43
  • 1
Polyclonal

Conjugué

  • 28
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TRIP4 est non-conjugé

Application

  • 31
  • 20
  • 9
  • 6
  • 6
  • 3
  • 2
  • 1
  • 1
Immunohistochemistry (IHC)
  • Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human TRIP4 (NP_057297.2).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    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

    TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

    Autre désignation

    TRIP4

    Sujet

    TRIP4,ASC-1,ASC1,HsT17391,MDCDC,SMABF1,ZC2HC5,This gene encodes a subunit of the tetrameric nuclear activating signal cointegrator 1 (ASC-1) complex, which associates with transcriptional coactivators, nuclear receptors and basal transcription factors to facilitate nuclear receptors-mediated transcription. This protein is localized in the nucleus and contains an E1A-type zinc finger domain, which mediates interaction with transcriptional coactivators and ligand-bound nuclear receptors, such as thyroid hormone receptor and retinoid X receptor alpha, but not glucocorticoid receptor. Mutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1).

    ID gène

    9325

    UniProt

    Q15650
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