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GALT anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement GALT dans WB. Il présente une réactivité envers Humain, Rat et Souris.
N° du produit ABIN631216

Aperçu rapide pour GALT anticorps (C-Term) (ABIN631216)

Antigène

Voir toutes GALT Anticorps
GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

Reactivité

  • 48
  • 17
  • 12
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 43
  • 10
Lapin

Clonalité

  • 41
  • 12
Polyclonal

Conjugué

  • 27
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp GALT est non-conjugé

Application

  • 36
  • 17
  • 10
  • 8
  • 8
  • 6
  • 6
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 14
    • 8
    • 5
    • 1
    • 1
    • 1
    C-Term

    Specificité

    GALT antibody was raised against the C terminal of GALT

    Purification

    Affinity purified

    Immunogène

    GALT antibody was raised using the C terminal of GALT corresponding to a region with amino acids LLRSATVRKFMVGYEMLAQAQRDLTPEQAAERLRALPEVHYHLGQKDRET
  • Indications d'application

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

    Commentaires

    GALT Blocking Peptide, (ABIN5613721), is also available for use as a blocking control in assays to test for specificity of this GALT antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GALT 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

    GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

    Autre désignation

    GALT

    Sujet

    Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet.

    Poids moléculaire

    43 kDa (MW of target protein)
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