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Leadgene Leadgene
Lactate Oxidase (LOX)
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Catalog Number

LDG0033RG

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  • Specifications
    • Expression system

      Escherichia coli

      Activity

      ≥200 U/mg

    • Unit Definition

      One unit causes the formation of one micromole of hydrogen peroxide (half a micromole of quinoneimine dye) per minute under the conditions described below.

      Form

      Lyophilized (Yellowish amorphous powder)

  • Background
    • Synonyms

      LOX, LctO, Lactic oxygenase, Lactic oxidase, Lactate monooxygenase, L-lactate oxidase

  • Instruction
    • Reconstitution

      It is recommended to weight and reconstitute 10 mg of lyophilized powder in 200 μL double-distilled water directly (final activity is 10 U/ μL) and incubate the solution for at least 10 mins to ensure sufficient re-dissolved.

      Shipping

      The product is shipped with polar packs. Upon receipt, store it immediately at -20°C or lower for long term storage.

    • Stability & Storage

      This product is stable at -20°C for long-term storage under sterile conditions.
      Avoid repeated free-thaw cycles.

  • Image
    pH stability of LOX. The enzyme powder was reconstituted by double-distilled water and treated with different pH buffer condition at 25°C for 16 hours. pH 4.0-6.0, 0.1 M Sodium citrate buffer; pH 7.5-8.0, 0.1 M Potassium phosphate buffer; pH 8.5, 0.1 M Tris-HCl buffer; pH 10.0-11.0, 0.1 M Carbonate-bicarbonate buffer.

    pH stability of LOX.
    The enzyme powder was reconstituted by double-distilled water and treated with different pH buffer condition at 25°C for 16 hours. pH 4.0-6.0, 0.1 M Sodium citrate buffer; pH 7.5-8.0, 0.1 M Potassium phosphate buffer; pH 8.5, 0.1 M Tris-HCl buffer; pH 10.0-11.0, 0.1 M Carbonate-bicarbonate buffer.

    Thermal stability of LOX. The enzyme powder was reconstituted by double-distilled water and treated with different temperatures for 10 minutes. Final concentration: 10 U/ mL.

    Thermal stability of LOX.
    The enzyme powder was reconstituted by double-distilled water and treated with different temperatures for 10 minutes. Final concentration: 10 U/ mL.

    pH activity of LOX. The buffer conditions with various pH values were used in the reaction at 37°C. pH 4.0-6.0, 0.1 M Sodium citrate buffer; pH 7.5-8.0, 0.1 M Potassium phosphate buffer; pH 8.5, 0.1 M Tris-HCl buffer; pH 10.0-11.0, 0.1 M Carbonate-bicarbonate buffer.

    pH activity of LOX.
    The buffer conditions with various pH values were used in the reaction at 37°C. pH 4.0-6.0, 0.1 M Sodium citrate buffer; pH 7.5-8.0, 0.1 M Potassium phosphate buffer; pH 8.5, 0.1 M Tris-HCl buffer; pH 10.0-11.0, 0.1 M Carbonate-bicarbonate buffer.

    Temperature activity of LOX. The enzyme reactions in 20 M K-Phosphate buffer, pH 7.5, were carried out under different temperatures.

    Temperature activity of LOX.
    The enzyme reactions in 20 M K-Phosphate buffer, pH 7.5, were carried out under different temperatures.

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