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Hexosaminidase A anticorps

Cet anticorps anti-Hexosaminidase A est un anticorps Souris Monoclonal détectant Hexosaminidase A dans WB, FACS et EIA. Adapté pour Humain.
N° du produit ABIN1105521

Aperçu rapide pour Hexosaminidase A anticorps (ABIN1105521)

Antigène

Voir toutes Hexosaminidase A (HEXA) Anticorps
Hexosaminidase A (HEXA)

Reactivité

  • 59
  • 25
  • 15
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 48
  • 15
Souris

Clonalité

  • 50
  • 13
Monoclonal

Conjugué

  • 42
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Hexosaminidase A est non-conjugé

Application

  • 52
  • 33
  • 15
  • 8
  • 7
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)

Clone

3F10
  • Specificité

    Recognizes Beta-hexosaminidase alpha / HEXA

    Réactivité croisée (Details)

    Species reactivity (tested):Human.

    Purification

    Purified

    Isotype

    IgG2b
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.0 mg/mL

    Buffer

    PBS, 0.05 % Sodium Azide, 0.5 % protein stabilizer

    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.
  • Antigène

    Hexosaminidase A (HEXA)

    Autre désignation

    beta-Hexosaminidase alpha / HEXA

    Sujet

    This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I).Synonyms: Beta-N-acetylhexosaminidase subunit alpha, N-acetyl-beta-glucosaminidase subunit alpha

    Poids moléculaire

    60.7 kDa

    ID gène

    3073

    Pathways

    Sensory Perception of Sound, Glycosaminoglycan Metabolic Process
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