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

Ubiquitin hydrolase 1 anticorps

L’anticorps anti-Ubiquitin hydrolase 1 Monoclonal Souris est utilisé pour la détection de Ubiquitin hydrolase 1 dans des échantillons de Humain, Boeuf (Vache), Souris et Rat. Il a été validé pour WB et IHC.
N° du produit ABIN5688748
792,00 €
Plus frais de livraison 40,00 € et TVA
0.1 mL
Destination: France
Envoi sous 6 à 8 jours ouvrables

Aperçu rapide pour Ubiquitin hydrolase 1 anticorps (ABIN5688748)

Antigène

Ubiquitin hydrolase 1

Reactivité

Humain, Boeuf (Vache), Souris, Rat

Hôte

  • 1
  • 1
Souris

Clonalité

  • 1
  • 1
Monoclonal

Conjugué

  • 2
Inconjugué

Application

  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

Clone

MCA-BH7
  • Specificité

    Specific for the ~24  kDa UCHL1 protein.

    Purification

    Total IgG fraction

    Immunogène

    Recombinant full length human UCHL1 purified from E. coli.

    Isotype

    IgG1
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Stock

    -20 °C

    Stockage commentaire

    Ubiquitin Hydrolase 1 antibody can be stored at -20°C and is stable at -20°C for at least 1 year.
  • Antigène

    Ubiquitin hydrolase 1

    Sujet

    Ubiquitin C-terminal hydrolase 1 (UCHL1) is also known as ubiquitin carboxyl esterase L1, ubiquitin thiolesterase, neuron-specific protein PGP9.5 and Park5. It was originally identified as a major component of the neuronal cytoplasm from 2-dimensional gel analysis of brain tissues, and was given the name PGP9.5. It was later found that ubiquitin C-terminal hydrolase enzyme activity was associated with the PGP9.5 protein. The ubiquitin C-terminal hydrolases cleave ubiquitin from other molecules. Regulation of the ubiquitin pathway is very important and many disease states are associated with defects in this pathway. Genetic knockout of UCHL1 in mice results in a motor neuron degeneration similar to the spontaneous gracile axonal dystrophy (gad) mutant mice. Point mutations in the UCHL1 gene are associated with some forms of human Parkinson's disease. Since UCHL1 is heavily expressed in neurons, it is released in large amounts following injury or degeneration, so the detection of UCHL1 in CSF and other bodily fluids can be used as a biomarker.

    Poids moléculaire

    24 kDa

    ID gène

    7345

    UniProt

    P09936
Vous êtes ici:
Chat with us!