FUS anticorps

N° du produit ABIN7880833

Cet anticorps anti-FUS Polyclonal Lapin (ABIN7880833) détecte spécifiquement FUS dans WB, IF, FACS et IHC (p). L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour FUS anticorps (ABIN7880833)

Antigène: FUS (Fused in Sarcoma (FUS))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FUS est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-FUS anticorps

Fonction: TLS Antibody / Translocated in liposarcoma protein / FUS

Séquence: ENVTIESVAD YFKQ

Purification: Antigen affinity purified

Immunogène: Amino acids ENVTIESVADYFKQ from the human protein were used as the immunogen for the TLS antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the TLS antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the TLS antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur FUS

Antigène: FUS (Fused in Sarcoma (FUS))

Autre désignation: TLS

Sujet: RNA-binding protein FUS/TLS (Fused in Sarcoma/Translocated in Sarcoma) is a protein that in humans is encoded by the FUS gene. This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6.

UniProt: P35637