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The process of removing the contaminants in the environment by biological methods using the metabolic potential of microorganisms to degrade a wide variety of pollutants has been explored with some success.
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Synthesis of silver nanoparticles is achieved by several physical, chemical and biological methods using top-down or bottom-up approaches [2, 12, 13, 14, 15, 16, 17, 18].
In this study, AgNPs synthesized were of average size 8 20 nm and zeta potential of −7.23 mV by the biological method using a technique involving electrostatic interaction between positively charged amino group in the extract and negatively charged Ag ions, producing negatively charged AgNPs.
Pro-hormone fragments (pro-ADM) are more stable than the complete peptide and their levels can be measured in biological fluids by automated methods using the TRACE (Time-Resolved Amplified Cryptate Emission) method after immuno-capture.
Prohormone fragments (pro-ADM) are more stable than the complete peptide and their levels can be measured in biological fluids by automated methods using the TRACE (Time-Resolved Amplified Cryptate Emission) method after immunocapture.
Hence, we validated the differential expression of 115 genes, randomly selected from the list of DEGs that were identified by the four methods, using independent biological replicates and high-throughput quantitative reverse-transcription PCR (qPCR).
The comparison of real-time PCR data to that obtained in the microarray analysis showed the same trend and a strong correlation between the data obtained by the two methods using different biological samples, suggesting that the transcriptional profiles derived from the microarray data are accurate and reproducible.
Selected α-aminophosphonates were entered into a biological assay test and were studied by docking methods, using Autodock 3.0.
We then assessed the biological implications of temporal clustering in both treatments and by both clustering methods, using gene ontology and pathway tools.
In summary, we have synthesized the multifunctional RNase A@C-dots particles by one-step microwave method using the biological molecule of RNase A as an assistant reagent.
The promotion mirrors methods used by Associated Newspaper.
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