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Arylsulfatase A anticorps

L’anticorps Lapin Polyclonal anti-Arylsulfatase A a été validé pour WB, FACS et IHC (p). Il convient pour détecter Arylsulfatase A dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN4950226

Aperçu rapide pour Arylsulfatase A anticorps (ABIN4950226)

Antigène

Voir toutes Arylsulfatase A (ARSA) Anticorps
Arylsulfatase A (ARSA)

Reactivité

  • 51
  • 34
  • 33
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 48
  • 17
  • 1
Lapin

Clonalité

  • 51
  • 15
Polyclonal

Conjugué

  • 34
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Arylsulfatase A est non-conjugé

Application

  • 49
  • 18
  • 16
  • 13
  • 13
  • 9
  • 8
  • 7
  • 5
  • 5
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Purification

    Antigen affinity

    Immunogène

    Amino acids QALKQLQLLKAQLDAAVTFGPSQVARGED of human ARSA were used as the immunogen for the ARSA antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the ARSA antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the ARSA antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    Arylsulfatase A (ARSA)

    Autre désignation

    ARSA

    Sujet

    Arylsulfatase A (ARSA) is an enzyme that breaks down sulfatides, namely cerebroside 3-sulfate intocerebroside and sulfate. In humans, arylsulfatase A is encoded by the ARSA gene. ARSA is mapped to 22q13.33. The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.

    UniProt

    P15289
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