Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

TSEN34 anticorps (AA 1-310)

L’anticorps anti-TSEN34 Polyclonal Lapin est utilisé pour la détection de TSEN34 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, IF et ELISA.
N° du produit ABIN7869177
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour TSEN34 anticorps (AA 1-310) (ABIN7869177)

Antigène

Voir toutes TSEN34 Anticorps
TSEN34 (tRNA Splicing Endonuclease 34 Homolog (TSEN34))

Reactivité

Humain, Souris, Rat

Hôte

  • 3
  • 3
Lapin

Clonalité

  • 6
Polyclonal

Conjugué

  • 6
Cet anticorp TSEN34 est non-conjugé

Application

  • 6
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), ELISA
  • Épitope

    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-310

    Fonction

    TSEN34 Antibody / tRNA-splicing endonuclease subunit Sen34

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids M1-Q310) was used as the immunogen for the TSEN34 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the TSEN34 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • 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 TSEN34 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    TSEN34 (tRNA Splicing Endonuclease 34 Homolog (TSEN34))

    Autre désignation

    TSEN34

    Sujet

    TRNA-splicing endonuclease subunit Sen34 is an enzyme that in humans is encoded by the TSEN34 gene. This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    UniProt

    Q9BSV6
Vous êtes ici:
Chat with us!