SINGLE-USE, DISPOSABLE HIGH-PRESSURE LIQUID CHROMATOGRAPHY COLUMNS FOR HIGH-THROUGHPUT ANALYSISA device for separating one or more molecules of interest in a liquid specimen including a monolithic body defining a fractionation column. The column includes an inlet opening at a proximal end of the ...
It is demonstrated how for a virus clearance study for a multispecific antibody, the continuous protein A capture chromatography process, being run on multiple interconnected columns, can be mimicked with only a single column. With this mimicking small-scale model, resources and complexity can be ...
The XIC plot is a kind of time-signal chromatography plot of a specific m/z ion. 1.3.1.XIC overlay you can click on the checkbox besides the Ms2 feature for select different ion feature for create the XIC overlay plot: 1.4.TIC plot ...
Carbohydrate monolithic beds were synthesized in a single step in capillary columns to study affinity chromatography of lectins. In this method, carbohydrates (β-galactose, β-glucose, and α-mannose) with an easy to synthesize alkene terminated tetraethylene glycol spacer were used as functional mono...
Dr. Budnik will present an LC-MS workflow that allows researchers to perform proteomic and metabolomic analysis on the same type of chromatography simultaneously in parallel. Additionally, transcriptomic and genomic analysis can be added as extra options to get a “multi-omic analysis of ...
In this paper, an open-tubular capillary cell affinity chromatography (OT-CAC) method to enrich and separate target cells is described. Open tubular capillaries coated with anti-CD4, anti-CD14, or anti-CD19 antibodies were used as affinity chromatography columns to separate target blood cells. Ce...
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A nanoElute (Bruker) ultra-high-pressure nano-flow chromatography system was coupled to a trapped ion mobility–quadrupole time-of-flight mass spectrometer (timsTOF Pro, Bruker) with a CaptiveSpray nano-electrospray ion source (Bruker) equipped with an external column oven. Mobile phases A and B...
The resolution of fluorescence microscopy images is limited by the physical properties of light. In the last decade, numerous super-resolution microscopy (SRM) approaches have been proposed to deal with such hindrance. Here we present Mean-Shift Super Re
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