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Based on this, a new quantitative method for nucleic acid determination in aqueous solutions has been developed.
A method for nucleic acid amplification, loop-mediated isothermal amplification (LAMP) was employed to develop a rapid and simple detection system for periodontal pathogen, Porphyromonas gingivalis.
A method for nucleic acid amplification, loop-mediated isothermal amplification (LAMP) is a novel, sensitive and rapid technique, which can be applied for disease diagnosis in aquaculture.
In particular, rolling circle replication (RCR) has been introduced as a powerful method for nucleic acid synthesis.
The evolutionary distances were computed using Composite Likelihood method and the Poisson correction method for nucleic acid- and amino acid-based analysis respectively.
The method for nucleic acid aptamer selection is quite simple and yields highly specific aptamers within a short time [ 4, 6].
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The uses of nanoparticles and electrochemical and optical methods for nucleic acid detection have been explored extensively [1, 11, 12].
Concomitant improvements in methods for nucleic acid sequencing have led many investigators to characterize their clones by sequencing them.
Low and medium throughput laboratories now have an alternative to manual processes and spin-column methods for nucleic acid purification, thanks to a new automated system.
The development of rapid, cost-effective, sensitive and specific methods for nucleic acid detection is becoming more and more important, owing to their potential diverse applications in gene expression profiling, clinical disease diagnostics and treatment [1].
Thus, while molecular templates from FFPE tissues are of inferior quality as compared to their frozen counterparts, these may still be useable for a lot of recently developed methods for nucleic acid investigation, even microarray profiling and wide genome scans, while the main advantage from using molecular FFPE templates is accurate correlation of results with tissue histology.
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