Determine the necessary mass, volume, or concentration for preparing a solution.
Bioactive, Recombinant, EnzymoPure™, expressed in E.coli; ≥0.5 U/mg protein; Protein concentration: See COA Bioactive,Recombinant,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.
Sucrose synthase (OcSUS1), E.C 2.4.1.13, derived from Ornithogalum caudatum. This enzyme is applied for the synthesis of UDP-glucose. The product is recombinantly expressed in Escherichia coli with high purity and suitable for one-pot multi-enzyme systems.
Reaction Equation
Neu5Ac + CTP —— CMP-Neu5Ac + PPi
Usage Instructions
1.Add substrates and 5 mM MgCl₂ to the reaction system. Supplement buffer salts (e.g., Tris-HCl) as needed to adjust pH to 7, then add an appropriate amount of OcSUS1 according to reaction requirements.
2.Mix thoroughly and incubate the sample at 37 °C for 1–2 h. Tris-HCl (pH 7) is the recommended reaction buffer; most common biological buffers such as Tris and PBS are also compatible.
3.Terminate the reaction by heat inactivation in a boiling water bath for 5 min, centrifuge at 12,000 rpm for 10 min, and collect the supernatant for detection.
Notes
For scale-up reactions, incubation duration or enzyme dosage shall be adjusted based on actual conditions; gentle shaking is recommended for uniform mixing.
Most conventional biological buffers including Tris and PBS are applicable. Buffers outside this pH range (e.g., acetate buffer) may also work, yet incubation time and enzyme loading need to be optimized experimentally.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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