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GM2A anticorps (N-Term)

Cet anticorps anti-GM2A est un anticorps Lapin Polyclonal détectant GM2A dans WB. Adapté pour Humain.
N° du produit ABIN632538

Aperçu rapide pour GM2A anticorps (N-Term) (ABIN632538)

Antigène

Voir toutes GM2A Anticorps
GM2A (GM2 Ganglioside Activator (GM2A))

Reactivité

  • 56
  • 20
  • 19
  • 1
  • 1
Humain

Hôte

  • 48
  • 8
  • 2
Lapin

Clonalité

  • 52
  • 6
Polyclonal

Conjugué

  • 27
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GM2A est non-conjugé

Application

  • 44
  • 23
  • 13
  • 13
  • 12
  • 5
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 6
    • 6
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    GM2 A antibody was raised against the N terminal of GM2

    Purification

    Affinity purified

    Immunogène

    GM2 A antibody was raised using the N terminal of GM2 corresponding to a region with amino acids SWDNCDEGKDPAVIRSLTLEPDPIIVPGNVTLSVMGSTSVPLSSPLKVDL
  • Indications d'application

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Commentaires

    GM2A Blocking Peptide, (ABIN5613801), is also available for use as a blocking control in assays to test for specificity of this GM2A antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GM0 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène

    GM2A (GM2 Ganglioside Activator (GM2A))

    Autre désignation

    GM2A

    Sujet

    This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    18 kDa (MW of target protein)
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