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

ASL anticorps

Cet anticorps anti-ASL est un anticorps Lapin Polyclonal détectant ASL dans IHC et IF. Adapté pour Humain et Souris.
N° du produit ABIN7262160

Aperçu rapide pour ASL anticorps (ABIN7262160)

Antigène

Voir toutes ASL Anticorps
ASL (Argininosuccinate Lyase (ASL))

Reactivité

  • 58
  • 14
  • 11
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
Humain, Souris

Hôte

  • 53
  • 5
Lapin

Clonalité

  • 55
  • 3
Polyclonal

Conjugué

  • 29
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ASL est non-conjugé

Application

  • 40
  • 13
  • 13
  • 12
  • 11
  • 10
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human ASL (NP_000039.2).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200 IF 1:50-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    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.
  • Antigène

    ASL (Argininosuccinate Lyase (ASL))

    Autre désignation

    ASL

    Sujet

    This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

    ID gène

    435

    UniProt

    P04424

    Pathways

    Response to Growth Hormone Stimulus
Vous êtes ici:
Chat with us!