Samples were processed using mass-spectrometry coupled with reversed-phase ultra-performance liquid chromatography (UPLC-MS) (ACQUITY UPLC System; Waters, USA) in positive and negative ionization modes in Q-TOF Maxis Impact II, Bruker Daltonik, Germany. Settings: Ion Polarity: positive/negative, Scan mode: MS, Mass range: 50 -1200 m/z, Spectra rate: 2 Hz. UPLC separation was performed on the C8 Acquity Beh column (2.1 mm Х 100 mm, 1.7-μm particle size; Waters) and the Acquity BEH C8 1.7 μm Vanguard precolumn (Waters) at 60 °C. The detailed information can be found in Methods S3. Previously we have validated the extraction and profiling technique for FAs [56 (link)] and TAGs [57 ] in sunflower.
Mass spectrometry Reversed phase liquid chromatography Scan Sunflower
Corresponding Organization : Skolkovo Institute of Science and Technology
Other organizations :
University of Southern California, All-Russian Research Institute of Oil Crops by V.S. Pustovoit, All-Russian Rice Research Institute, N.I. Vavilov Research Institute of Plant Industry
Mass-spectrometry coupled with reversed-phase ultra-performance liquid chromatography (UPLC-MS)
dependent variables
Metabolite profiles
control variables
Ion Polarity: positive/negative
Scan mode: MS
Mass range: 50 -1200 m/z
Spectra rate: 2 Hz
UPLC separation on the C8 Acquity Beh column (2.1 mm Х 100 mm, 1.7-μm particle size; Waters) and the Acquity BEH C8 1.7 μm Vanguard precolumn (Waters) at 60 °C
positive controls
The extraction and profiling technique for FAs and TAGs in sunflower has been previously validated [56, 57]
Annotations
Based on most similar protocols
Etiam vel ipsum. Morbi facilisis vestibulum nisl. Praesent cursus laoreet felis. Integer adipiscing pretium orci. Nulla facilisi. Quisque posuere bibendum purus. Nulla quam mauris, cursus eget, convallis ac, molestie non, enim. Aliquam congue. Quisque sagittis nonummy sapien. Proin molestie sem vitae urna. Maecenas lorem.
As authors may omit details in methods from publication, our AI will look for missing critical information across the 5 most similar protocols.
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to
get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required