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

ABHD5 anticorps

L’anticorps Lapin Monoclonal anti-ABHD5 a été validé pour WB. Il convient pour détecter ABHD5 dans des échantillons de Humain.
N° du produit ABIN7265357

Aperçu rapide pour ABHD5 anticorps (ABIN7265357)

Antigène

Voir toutes ABHD5 Anticorps
ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

Reactivité

  • 37
  • 10
  • 9
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
Humain

Hôte

  • 28
  • 9
  • 1
Lapin

Clonalité

  • 28
  • 10
Monoclonal

Conjugué

  • 25
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ABHD5 est non-conjugé

Application

  • 25
  • 14
  • 11
  • 7
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    ABHD5 Rabbit mAb

     Réactivité croisée

    Humain, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human ABHD5

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

    Autre désignation

    ABHD5

    Sujet

    The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation. [provided by RefSeq, Jul 2008],CDS, CGI58, IECN2, NCIE2,Cancer,Cardiovascular,Endocrine & Metabolism,Endocrine and metabolic diseases,Endocrine and metabolic diseases_Obesity,Lipid Metabolism,Lipids,Lipids_Adipose Related,Lipids_Fatty Acids,Signal Transduction,ABHD5

    Poids moléculaire

    45kDa

    ID gène

    51099

    UniProt

    Q8WTS1

    Pathways

    Lipid Metabolism
Vous êtes ici:
Chat with us!