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HAL anticorps

Cet anticorps anti-HAL est un anticorps Lapin Polyclonal détectant HAL dans WB. Adapté pour Humain.
N° du produit ABIN7466882

Aperçu rapide pour HAL anticorps (ABIN7466882)

Antigène

Voir toutes HAL Anticorps
HAL (Histidine Ammonia-Lyase (HAL))

Reactivité

  • 19
  • 9
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 16
  • 3
Lapin

Clonalité

  • 18
  • 1
Polyclonal

Conjugué

  • 15
  • 2
  • 1
  • 1
Cet anticorp HAL est non-conjugé

Application

  • 14
  • 9
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB)
  •  Réactivité croisée

    Souris

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein encompassing a sequence within the center region of human HAL. The exact sequence is proprietary.

    Isotype

    IgG
  • Indications d'application

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Commentaires

    Positive Control: Mouse liver

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Antigène

    HAL (Histidine Ammonia-Lyase (HAL))

    Autre désignation

    histidine ammonia-lyase

    Sujet

    Histidine ammonia-lyase , HIS , HSTD,Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids [provided by RefSeq]

    Poids moléculaire

    73 kDa

    ID gène

    3034

    UniProt

    P42357
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