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ACAT1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement ACAT1 dans WB. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN631042

Aperçu rapide pour ACAT1 anticorps (ABIN631042)

Antigène

Voir toutes ACAT1 Anticorps
ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Reactivité

  • 68
  • 35
  • 29
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 61
  • 5
  • 4
Lapin

Clonalité

  • 60
  • 10
Polyclonal

Conjugué

  • 43
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ACAT1 est non-conjugé

Application

  • 41
  • 28
  • 26
  • 13
  • 13
  • 11
  • 9
  • 8
  • 7
  • 3
  • 3
  • 2
Western Blotting (WB)
  • Purification

    Affinity purified

    Immunogène

    ACAT1 antibody was raised using a synthetic peptide corresponding to a region with amino acids SYTRSKAAWEAGKFGNEVIPVTVTVKGQPDVVVKEDEEYKRVDFSKVPKL
  • Indications d'application

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

    Commentaires

    ACAT1 Blocking Peptide, (ABIN5611882), is also available for use as a blocking control in assays to test for specificity of this ACAT1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ACAT1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    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

    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

    Autre désignation

    ACAT1

    Sujet

    ACAT1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. The gene encoding ACAT1 spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene are associated with the alpha-methylacetoaceticaciduria disorder, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.

    Poids moléculaire

    41 kDa (MW of target protein)
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