Sentence examples for methodology for isolation from inspiring English sources

A simple and highly sensitive analytical methodology for isolation and determination of patulin in apple-juice samples, based on enzyme-assisted extraction (EAE) and ionic liquid-based dispersive liquid liquid microextraction (IL-DLLME) was developed and optimized.

In this paper, we describe a methodology for isolation and recovery of ceramic or ceramic-like coating particles and metal wear particles from serum lubricants under ultra-low and low wear performance.

We unequivocally established the methodology for isolation, identification, and characterization of a novel fungal endophyte (Trametes hirsuta) that produces aryl tetralin lignans consistently as shown by HPLC, LC MS, LC/MS MS and 1H NMR.

In this manner, we present a methodology for isolation of individual strains from mixed C. difficile samples, quantification of antibiotic treatments, and the engineering of nutrient environments to control microbiomes.

In this regard, the article titled "'Adherent' versus Other Isolation Strategies for Expanding Purified, Potent, and Activated Human NK Cells for Cancer Immunotherapy" by S. R. Selvan and J. P. Dowling introduces a simple methodology for isolation and expansion of NK cells for adoptive cell therapies.

There are a number of confounding factors that obstruct a fair comparison on the work presented here and that of Bunnik et al. These factors include the strain, the time points sampled, the methodology for isolation of polysomes, and most importantly, the overall sequencing coverage.

Simple and reliable methodologies for isolation, detection, characterization and enumeration of somatic and F-specific bacteriophage are available in the literature.

Fig. 4 Methodologies for isolation and identification of CTCs or DTCs.

The different methodologies for isolation, culture and analysis of muscle-derived cells by different laboratories have made it extremely difficult to make comparisons between the studies.

Despite the fact that technologies for RNA isolation have shown tremendous improvements over the past decade with RNA isolation kits for tissue, cells as well as whole blood, there is still no commercially available methodology for the isolation of good quality RNA from microliter volumes of human whole blood suitable for gene expression profiling on DNA microarrays.

In this review, we summarize methodology for the isolation and phenotypic characterization of macrophages and DCs from the mouse intestine and discuss how this may be useful for gaining insight into the mechanisms by which mucosal immune tolerance is maintained.