TRIP4 anticorps

N° du produit ABIN7384096

Détail du produit anti-TRIP4 anticorps

Antigène: TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TRIP4 est non-conjugé

Application: Immunohistochemistry (IHC)

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

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.

Détails sur TRIP4

Antigène: TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))

Autre désignation: TRIP4 (TRIP4 Produits)

Synonymes: anticorps TRIP4, anticorps ASC-1, anticorps ASC1, anticorps HsT17391, anticorps im:7143009, anticorps si:busm1-221i3.1, anticorps si:dkey-173l11.4, anticorps zgc:153348, anticorps 4930558E03Rik, anticorps Asc1, anticorps BB191711, anticorps thyroid hormone receptor interactor 4, anticorps thyroid hormone receptor interactor 4 L homeolog, anticorps TRIP4, anticorps TREPR_2022, anticorps trip4, anticorps trip4.L, anticorps 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