Determine the necessary mass, volume, or concentration for preparing a solution.
EnzymoPure™, BioReagent, ≥90%(SDS-PAGE), ≥ 4 U/mg BioReagent,EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Avoid repeated freezing and thawing Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
It is used in the research and development of enzymatic glycosylated albumin reagents and mass formulation.
Enzymatic properties
Source: Microorganism
Enzymology Committee Number: EC1.5.3
Molecular weight: 55kDa (SDS-PAGE)
Isoelectric point: 6
Km value: 5.0×10
⁻⁴
M (Fructosyl-Ala)
Inhibitors: Hg
²⁺
, Pb
²⁺
Optimal pH: 7.7 Figure 1
Optimum temperature: 42℃ Figure 2
pH stability: 5.0-9.5 (25℃, 16h) Figure 3
Thermal stability: Stable below 40℃ (pH8.0, 30min) Figure 4
Stability: -25 ~ -15℃ standing store for 12 months
More than 90% activity Figure 5
Protective agent: glycerin, trehalose





Assay method for activity
1. Principle
2. Definition of enzyme activityUnit enzyme activity is defined as the amount of enzyme required to catalyze the production of 1μmol H2O2 per minute under the following conditions.
3. Reagent preparation
Reagent I: 1M potassium phosphate buffer, pH8.0
Reagent II: 1kU/mL POD
Reagent III: 50mM TOOS solution
Reagent IV: 50mM 4-AA solution
Reagent V: 200mM Glycated alanine
Enzyme diluent: 20mM Tris-HCl, pH8.0
Prepare the reaction mixture as follows:
Reagent I: 10mL
Reagent II: 0.1mL
Reagent III: 1mL
Reagent IV: 1mL
Reagent V: 10mL
Double steam water set volume to 100mL
4. Operation procedure
4.1 Add 980μL reaction mixture into 1mL colorimetric dish.
4.2 Incubate at 37°C for 5 minutes.
4.3 Add 20 μL of enzyme solution to be tested to the reaction mixture.
4.4 Reaction at 37°C, the absorbance change (∆As) of the sample within 1min is detected by spectrophotometer at 555nm.
* Blank control measurement method: Use 20 μL of enzyme dilution solution instead of the enzyme solution to be tested, and measure the absorbance change (ΔAb) of the sample within 1 minute.
∆A=∆As-∆Ab
5. Vitality computing
Vt: Total volume of reaction liquid (1.0 mL);
Vs: Enzyme liquid volume (0.02 mL);
t: Reaction time (1 min);
df: Dilution ratio;
C: Enzyme concentration (mg/mL);
1.0: Optical path length (cm);
1/2: 1 mole hydrogen peroxide to generate 1/2 mole quinone imide dye;
39.2: Under standard reaction conditions, the millimolar absorption coefficient of the color group at 555nm (cm²
/μmol).
Comprehensive hazard, handling, storage, and regulatory compliance document.
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| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Feb 24, 2026 | rp216165 |
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