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This work assays for the first time the potential effect of an antibiotic of agricultural use (oxytetracycline, OTC) on the performance of a biomixture (biologically active core of BPS), considering that antibiotic-containing wastewaters are also produced in agricultural labors.
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In this work, injection assays have been carried out with fluids comprising microemulsion-based commercial anionic surfactants, oil from the Quiambina Field (mature field in the Brazilian State of Bahia) and brine (2% KCl).
In this work, injection assays have been carried out with two types of microemulsion: one was prepared with a commercial surfactant (MCS) and another contained a surfactant synthesized in laboratory (MLS).
During this work, uptake assays of radioactive nucleotides has been performed and showed a time dependent uptake of ATP.
A novel strategy for the fabrication of an electrochemical aptasensor is proposed; this strategy has been employed in this work to assay thrombin concentration.
As shown in previous studies and in this work, BD GeneOhm™ MRSA assay is both specific and sensitive [ 1, 10, 14- 17].
In this work we assayed the capacity of the Junin Z protein as a VLP-forming protein carrying the green fluorescent protein (eGFP) as a model antigen.
In this work we assayed the capacity of Junin Z protein to produce VLPs carrying the green fluorescent protein (eGFP), as a model antigen.
In this work, MNase assay was used to digest linker DNA regions resulting in mononucleosomal DNA fragments of length ∼150 bp.
In this work we performed assays for the genetic improvement of the oleaginous yeast Lipomyces starkeyi DSM 70296 focusing on its utilization for lipid biosynthesis from renewable sources.
Therefore in this work, a killing assay was performed, evaluating the impact of several cell inactivation techniques with various modes of action on EMA/PMA-qPCR results.
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CEO of Professional Science Editing for Scientists @ prosciediting.com