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The Aurora® Elite™ 15 cm x 150 μm column is perfect for faster separation, at higher flowrates, whilst maintaining reproducible and high resolution peptide separation.
Peak characteristics

Figure 1: Example peaks were chosen across the 1.5μl/min 30 min gradient. All peaks show excellent FWHM and symmetry through the entire gradient.
Figure 2: Asymmetry factors were calculated for all identified peptides, and plotted on a density plot. The Median asymmetry was equal the 1, indicating that a majority of peaks show a Gaussian distribution.
Reproducibility
CV by gradient and flow rate

Figure 3: HeLa tryptic digest was run on an Aurora Elite 15 cm x 150 μm column. Gradients 10min, 15min, 30min and 45min were run at flowrates 0.4 ul/min and 1.5 ul/min (4 replicates). Coefficient of variations of protein intensities were calculated across runs within each condition. Resulting calculations show sub 8% median CV across all samples.
METHODS
100ng of HeLa tryptic digest was introduced on an NCP3200 Ultimate 3000 LC, separated on an Aurora® Elite™ 15 cm x 150 μm column and Bruker Impact II Mass Spectrometer. Solvents were 0.1% formic acid as solvent A and 99.9% Acetonitrile as solvent B. Capillary voltage was set to 1800V, m/z range 200-2000. With AutoMS/MS on, and cycle time 0.5sec.
R E A D I N G
For further resources and technical support, visit our Help Centre at helpcentre.ionoptickscopy.com. To view other application notes, read the latest publications featuring Aurora Series columns, or view the full range of IonOpticks products, visit our website at www.ionoptickscopy.com

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