For preparative HPLC, a LC-20AT chromatography system (Shimadzu, Kyoto, Japan) equipped with autosampler SIL-10AP, fraction collector FRC-10A and UV/vis detector SPD-20A was used. The separation column was a VP250/10 Nucleodur C18 HTec, 5 μm (Macherey Nagel). Method 2: 2-min focusing step with 30% acidified methanol in acidified water (0.1% (v/v) HCOOH), followed by a gradient linearly increasing in 33 min to 50% methanol, washing, and re-equilibration of the column (flow rate 3.5 ml min À 1 ). The detector was operating at 351 and 500 nm and the seven most abundant peaks at 351 nm were collected. Therefore, collection was performed between 24 and 50 min for peaks with higher intensity levels than 8000 μV.
Lc 20at chromatography system
The LC-20AT chromatography system is a high-performance liquid chromatography (HPLC) instrument manufactured by Shimadzu. It is designed for the separation, identification, and quantification of various chemical compounds in complex mixtures. The LC-20AT features a high-pressure pump, an auto-sampler, a column oven, and a variety of detectors, allowing for precise and reliable analytical results.
Lab products found in correlation
2 protocols using lc 20at chromatography system
Analytical and Preparative HPLC-PDA Protocol
For preparative HPLC, a LC-20AT chromatography system (Shimadzu, Kyoto, Japan) equipped with autosampler SIL-10AP, fraction collector FRC-10A and UV/vis detector SPD-20A was used. The separation column was a VP250/10 Nucleodur C18 HTec, 5 μm (Macherey Nagel). Method 2: 2-min focusing step with 30% acidified methanol in acidified water (0.1% (v/v) HCOOH), followed by a gradient linearly increasing in 33 min to 50% methanol, washing, and re-equilibration of the column (flow rate 3.5 ml min À 1 ). The detector was operating at 351 and 500 nm and the seven most abundant peaks at 351 nm were collected. Therefore, collection was performed between 24 and 50 min for peaks with higher intensity levels than 8000 μV.
Ligand Purity Determination by RP-HPLC
purity of the tested ligands was >95% as determined by analytical
RP-HPLC on a LC-20AT chromatography system (Shimadzu Corp.). A Waters
Atlantis T3 C18 column was used with a flow rate of 0.2
mL/min and a linear gradient from 0% to 45% solvent B over 45 min,
where solvent A was 0.05% TFA in H2O and solvent B was
0.043% TFA in 90/10% (v/v) ACN/ H2O. The UV absorbance
was monitored at 214 and 280 nm, with the 214 nm absorbance used to
calculate purity. Data were recorded and processed with LabSolutions
software (Shimadzu Corp.).
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