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In one, a complex purification procedure involving the isolation of exclusion bodies and their solubilization in urea resulted in purified soluble 37LRP [ 39].
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Our result was particularly good and interesting, as the product was recovered pure in short times and in excellent yield without requiring the use of complex purification procedures.
However, problems such as low protein expression level, lack of accurate post-translational modifications as well as complex purification procedures have made current approaches unsuitable for large-scale production.
In addition, three ribosomal proteins were co-purified with Nop1; ribosomal proteins are common false positives in protein complex purification procedures (Table 1)[ 31].
Although many of the reported methods are effective, but, some of them suffer from disadvantages such as harsh reaction conditions, use of hazardous solvents and toxic metals, long reaction times, complex working and purification procedures, long volume of catalyst loading and moderate yields.
A number of biotechnology products currently marketed are large molecules, produced from genetically modified mammalian cell lines, and extracted through complex and lengthy purification procedures [ 12, 13].
Multi-subunit membrane complexes can loose subunits during the purification procedure [44].
In this work, using multiple, dissimilar physico-chemical techniques, we demonstrate that the Escherichia coli RNA polymerase core enzyme obtained through a classic purification procedure forms stable (α2ββ'ω 2 complexes in the presence or absence of short DNA probes.
To enable biophysical studies of Bqt1 and Bqt2, we established a purification procedure for the Schizosaccharomyces japonicus Bqt1-Bqt2 complex, which is closely related to the S. pombe Bqt1 Bqt2 complex.
Because of the complex nature of faeces, an appropriate extraction and purification procedure was developed.
But no fluorescence signal was detected in control cells incubated with washed and ultra-filtrated transfection complexes (siRNA + LP + WF), confirming that the purification procedure used was sufficient to remove all non-associated with exosomes siRNA from the samples.
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