Amino Acid Analysis Solutions | SHIMADZU EUROPA
New UF-Amino Station Offers Simultaneous Multicomponent Analysis for Enhanced Throughput
Analyze 38 amino acid components in just nine minutes!
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UF-Amino Station overcomes these limitations. Jointly developed by Shimadzu and Ajinomoto Co., Inc., it features a special-purpose, fast analysis column and a LCMS-2020 mass spectrometer, which supports ultra-fast analysis speeds, to achieve the simultaneous analysis of 38 amino acid and amino acid-related components* in just nine minutes. Additionally, it automates the derivatization reaction to eliminate the need for cumbersome pretreatment procedures by manual operation. UF-Amino Station is an excellent tool for the analysis of food products, such as meat and fermented foods containing many impurity components, and for the biochemical analysis of culture fluid. * Permits the analysis of 38 amino acid-related components, such as anserine, citrulline, taurine, and GABA (γ-aminobutyric acid), in addition to the 20 major amino acid components. |
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Opening Up a New World of Amino Acid Analysis
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LC/MS Offers Superb Detection Selectivity
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AmiNaviTM Software Simplifies Operation
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Automated Derivatization Improves Efficiency and Reliability
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ApplicationsThe high selectivity of UF-Amino Station permits the analysis of amino acids in meat extract, which is difficult by PTC precolumn derivatization and UV detection due to the effects of impurity components. |
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Amino Acid Analysis in Commercial Serum-Free Medium (supplied by Ajinomoto Co. Inc.) |
Analysis of Amino Acids in Commercial Tea Drink |
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Analysis of Amino Acids in Commercial Beer |
Analysis of Amino Acids in Rat Blood Plasma |
Post-column Amino Acid Analysis System
For high-sensitivity measurement of amino acids in foods and biological samples
The analysis of amino acids plays an important role not only in the food industry, but also in natural product and pharmaceutical fields. This system uses detection by post-column fluorescence derivatization, with o-phthalaldehyde (OPA) / N-acetylcysteine as the reaction reagent, to selectively and sensitivly quantitate the amino acids contained in samples with high levels of contaminants.
Features
- Selectively detects amino acids based on Shimadzu’s highly acclaimed post-column reaction technology and high-sensitivity fluorescence detector.
- Determines amino acids with over ten times higher sensitivity than the ninhydrin method (UV detection), by using a derivatization method that provides a selective reaction with amino radicals in combination with fluorescence detection.
- Outstanding Reproducibility, as derivatization occurs after separation in the column, reactions are not affected by the sample matrix, resulting in exceptional precision of analyses.
- Easy to operate, since the eluent from the column is automatically derivatized by mixing it with the reaction reagent. This approach saves time and reduces manual labor.
- The mobile phase and reaction solution are available as a kit, reducing time and effort and minimizing variability due to their preparation.
Detection Principle
After amino acids are separated by cation exchange chromatography, aqueous sodium hypochlorite solution (to convert analytes to primary amines) and OPA/N-acetylcysteine reagent are added to the eluent, the resulting fluorescent derivatives are detected.
Analysis Example
Two models are available — a "Na" model, capable of rapidly analyzing amino acids hydrolyzed from protein, and a "Li" model, capable of separating naturally-occurring free amino acids. The chromatograms displayed below show the separation of a standard solution of hydrolyzed protein amino acids containing 17 components, measured using the "Na" model and the “Li” model results from analyzing soy sauce diluted by factor 200, respectively.
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