Uhplc-qe-ms

UHPLC-QE-MS (ultra-high-performance liquid chromatography–Q Exactive mass spectrometry) is an analytical platform that separates, identifies, and measures chemical compounds with high speed, mass accuracy, and resolution, making it valuable in modern medicine. UHPLC first resolves compounds according to their interactions with a chromatographic column under high pressure; electrospray ionization then converts them into ions, while the quadrupole selects ion populations and the Orbitrap measures their mass-to-charge ratios for accurate profiling and tandem MS analysis. The method supports drug and metabolite characterization, pharmacokinetic studies, metabolomics, impurity testing, and biomarker research, helping researchers investigate disease mechanisms and evaluate therapeutic responses.

Uhplc-qe-ms - Related Videos

Research

JoVE Journal - Chemistry

Simultaneous Measurement of HDAC1 and HDAC6 Activity in HeLa Cells Using UHPLC-MS

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Cited by 6 •

2017

The present method serves to identify isoform-specific inhibitors of histone deacetylases (HDAC) in HeLa cells by the UHPLC-MS analysis of multiple substrates. This is an antibody-free method developed to reflect HDAC1 and HDAC6 activity in the living cell environment, in contrast to single-isoform cell-free assays.

Research

JoVE Journal - Biology
Free Sample

FRET Imaging in Three-dimensional Hydrogels

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Cited by 3 •

2016

Förster resonance energy transfer (FRET) imaging is a powerful tool for real-time cell biology studies. Here a method for FRET imaging cells in physiologic three-dimensional (3D) hydrogel microenvironments using conventional epifluorescence microscopy is presented. An analysis for ratiometric FRET probes that yields linear ratios over the activation range is described.

Research

JoVE Journal - Biology
Free Sample

Discovering Protein Interactions and Characterizing Protein Function Using HaloTag Technology

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Cited by 11 •

2014

HaloTag technology is a multifunctional technology which has shown significant success in isolation of both small and large protein complexes from mammalian cells. Here we highlight the advantages of this technology compared to existing alternatives and demonstrate its utility to study numerous aspects of protein function inside eukaryotic cells.

A Strategy for Sensitive, Large Scale Quantitative Metabolomics

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Cited by 28 •

2014

Metabolite profiling has been a valuable asset in the study of metabolism in health and disease. Utilizing normal-phased liquid chromatography coupled to high-resolution mass spectrometry with polarity switching and a rapid duty cycle, we describe a protocol to analyze the polar metabolic composition of biological material with high sensitivity, accuracy, and resolution.

Printing Thermoresponsive Reverse Molds for the Creation of Patterned Two-component Hydrogels for 3D Cell Culture

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Cited by 60 •

2013

A bioprinter was used to create patterned hydrogels based on a sacrificial mold. The poloxamer mold was backfilled with a second hydrogel and then eluted, leaving voids which were filled with a third hydrogel. This method uses fast elution and good printability of poloxamer to generate complex architectures from biopolymers.

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