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In addition, it provides examples for detection and quantitation of environmental samples using QCM immunosensors.
Comparison of sequences from environmental samples using either degenerated or inosine containing amoA primers retrieved both identical and additional sequences.
The investigation of fungal species profiles directly from environmental samples using DGGE analysis of PCR-amplified SSU rDNA molecules can be used to improve the detection of fungal groups that are difficult to cultivate.
In the current study, for the first time, solid phase extraction combined with electro membrane extraction (SPE EME) was developed for ultra-preconcentration and determination of chlorophenoxy acid herbicides in environmental samples using capillary electrophoresis (CE).
Prior to hybridization analysis, the 16S 23S rDNA were amplified by polymerase chain reaction both from bacterial cells and environmental samples using two actinomycetes specific primers containing a 5′ biotin labeling.
Enzymatic analysis of microbial activity in water and other environmental samples using fluorescent synthetic substrates are well-established and highly sensitive methods in addition to providing a measure of specificity towards indicative bacteria.
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All uncultured, environmental samples used in this study are listed in Table S2.
Environmental samples, used for enrichment anaerobic cellulose degradation microflora, were collected from wheat straw compost, soil beneath wheat straw compost, rumen fluid, rumen solids, fresh cattle dung, rooted wood crumb, cattle dung compost, soil beneath cattle dung compost, and the activated sludge from wastewater digestion reactor.
In brief, metagenomics could be defined as the characterization of the vast number of genomes present in an environmental sample, using both a taxonomical and a functional analytical approach.
The proposed method was successfully demonstrated for on-line lead determination and applied in environmental water samples using an amount of 120 μL of chloroform as extractant and ammonium diethyldithiophosphate as chelating reagent.
Dr. Pollitt's research explores the human exposome through characterisation of environmental and biological samples using analytical and mass spectrometry (MS) techniques.
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