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Synergi 4 m max rp column

Manufactured by Phenomenex

The Synergi™ 4 μm Max-RP column is a reversed-phase high-performance liquid chromatography (HPLC) column. It features a particle size of 4 microns and a C18 bonded phase for the separation of a wide range of analytes.

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2 protocols using synergi 4 m max rp column

1

Quantification of Isomeric Aminobutyric Acids

Check if the same lab product or an alternative is used in the 5 most similar protocols
All components of liquid chromatography-tandem mass spectrometry (LC–MS/MS) system are from Shimadzu Scientific Instruments, Inc. (Columbia, MD). The LC system was equipped with pumps A and B (LC-30AD), and autosampler (SIL-30AC). The LC separation was conducted on a chiral SPP-TeicoShell column (150 × 4.6 mm, 2.7 µm, AZYP LLC., Arlington, TX) configured with a Synergi™ 4 µm Max-RP column as guard column (50 × 2.0 mm, Phenomenex, Torrance, CA). The MS/MS analysis was performed on Shimadzu LCMS-8050 triple quadrupole mass spectrometer.
Quantification of isomeric aminobutyric acids in human serum samples was followed the LC–MS/MS method as published previously21 (link). Briefly, mobile phases are methanol (A) and water containing 0.005% formic acid and 2.5 mM ammonium formate (B). The MS instrument was operated and optimized under positive electrospray (+ESI) and multiple reaction monitoring modes (MRM). The m/z transitions (precursor to product ions) and their tuning voltages were selected from published paper21 (link) and further optimized based on the best MRM responses from instrumental method optimization software. All analyses and data processing were completed on Shimadzu LabSolutions V5.91 software (Shimadzu Scientific Instruments, Inc., Columbia, MD).
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2

Quantification of Isomeric Aminobutyric Acids in Human Serum

Check if the same lab product or an alternative is used in the 5 most similar protocols
All components of LC–MS/MS system are from Shimadzu Scientific Instruments, Inc. (Columbia, MD). the LC system was equipped with pumps A and B (LC-30AD), and autosampler (SIL-30AC). The LC separation was conducted on a chiral SPP-TeicoShell column (150 × 4.6 mm, 2.7 µm, AZYP LLC., Arlington, TX) configured with a Synergi™ 4 µm Max-RP column as guard column (50 × 2.0 mm, Phenomenex, Torrance, CA). The MS/MS analysis was performed on Shimadzu LCMS-8050 triple quadrupole mass spectrometer.
Quantification of isomeric aminobutyric acids in human serum samples was followed the LC–MS/MS method published by our laboratory14 (link). Briefly, mobile phases are methanol (A) and water containing 0.005% formic acid and 2.5 mM ammonium formate (B). The MS instrument was operated and optimized under positive electrospray (+ ESI) and multiple reaction monitoring modes (MRM). The m/z transitions (precursor to product ions) and their tuning voltages were selected from our published paper14 (link) and further optimized based on the best MRM responses from instrumental method optimization software. All analyses and data processing were completed on Shimadzu LabSolutions V5.91 software (Shimadzu Scientific Instruments, Inc., Columbia, MD).
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