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PKLR anticorps (AA 1-230)

Cet anticorps Lapin Polyclonal détecte spécifiquement PKLR dans WB, IHC et IF. Il présente une réactivité envers Humain.
N° du produit ABIN1885816

Aperçu rapide pour PKLR anticorps (AA 1-230) (ABIN1885816)

Antigène

Voir toutes PKLR Anticorps
PKLR (Pyruvate Kinase, Liver and RBC (PKLR))

Reactivité

  • 61
  • 30
  • 22
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 59
  • 12
Lapin

Clonalité

  • 61
  • 10
Polyclonal

Conjugué

  • 39
  • 6
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp PKLR est non-conjugé

Application

  • 46
  • 32
  • 31
  • 9
  • 7
  • 5
  • 5
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Épitope

    • 14
    • 7
    • 7
    • 5
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-230

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 230 of Pyruvate Kinase(liver/RBC)
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    PKLR (Pyruvate Kinase, Liver and RBC (PKLR))

    Sujet

    The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis.Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA).Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq]

    Poids moléculaire

    62 kDa

    ID gène

    5313

    NCBI Accession

    NM_000298, NP_000289

    Pathways

    Ribonucleoside Biosynthetic Process
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