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Adenylate Kinase 1 anticorps (AA 149-189)

Cet anticorps Lapin Polyclonal détecte spécifiquement Adenylate Kinase 1 dans WB. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN5647008

Aperçu rapide pour Adenylate Kinase 1 anticorps (AA 149-189) (ABIN5647008)

Antigène

Voir toutes Adenylate Kinase 1 (AK1) Anticorps
Adenylate Kinase 1 (AK1)

Reactivité

  • 85
  • 23
  • 17
  • 8
  • 8
  • 8
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 80
  • 11
  • 6
Lapin

Clonalité

  • 87
  • 10
Polyclonal

Conjugué

  • 47
  • 10
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Adenylate Kinase 1 est non-conjugé

Application

  • 57
  • 35
  • 24
  • 22
  • 13
  • 13
  • 10
  • 10
  • 9
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 17
    • 15
    • 7
    • 7
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 149-189

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids 149-189 (RLETYYKATEPVIAFYEKRGIVRKVNAEGSVDSVFSQVCTH) from the human protein were used as the immunogen for the AK1 antibody.

    Isotype

    IgG
  • Indications d'application

    Western blot: 0.5-1 μg/mL

    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 AK1 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

    Adenylate Kinase 1 (AK1)

    Autre désignation

    AK1 / Adenylate Kinase 1

    Sujet

    This gene encodes an adenylate kinase enzyme involved in energy metabolism and homeostasis of cellular adenine nucleotide ratios in different intracellular compartments. This gene is highly expressed in skeletal muscle, brain and erythrocytes. Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.

    UniProt

    P00568

    Pathways

    Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process
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