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HGSNAT anticorps (N-Term)

Cet anticorps anti-HGSNAT est un anticorps Lapin Polyclonal détectant HGSNAT dans WB. Adapté pour Humain, Chien et Cheval.
N° du produit ABIN2790259

Aperçu rapide pour HGSNAT anticorps (N-Term) (ABIN2790259)

Antigène

Voir toutes HGSNAT Anticorps
HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))

Reactivité

  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Chien, Cheval

Hôte

  • 3
Lapin

Clonalité

  • 3
Polyclonal

Conjugué

  • 3
Cet anticorp HGSNAT est non-conjugé

Application

  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 1
    • 1
    N-Term

    Séquence

    RALAALLLAA SVLSAALLAP GGSSGRDAQA APPRDLDKKR HAELKMDQAL

    Homologie

    Dog: 86%, Horse: 82%, Human: 100%

    Attributs du produit

    This is a rabbit polyclonal antibody against HGSNAT. It was validated on Western Blot.

    Purification

    Affinity Purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human HGSNAT
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    Conseil sur la manipulation

    Avoid repeat freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Antigène

    HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))

    Autre désignation

    HGSNAT

    Sujet

    This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate.
    Protein Size: 219

    Poids moléculaire

    24 kDa

    ID gène

    138050

    UniProt

    Q8IVU6

    Pathways

    Glycosaminoglycan Metabolic Process
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