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In the last 15 years several methods have been developed to prepare molecular samples at temperatures well below 1 K and to completely control their translational degrees of freedom [1 4].
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The structure of end groups also affects the cloud point of PMAIPAC particularly for low molecular weight samples at low pH.
Data were acquired using the software Clampex 9.2 (Molecular Device), sampled at 20 kHz and filtered at 10 kHz.
Due to the difficulty in loading the sample in the shape of a perfect cylinder and almost certain inhomogeneity of the samples at molecular level, at least 20 replicate measurements were performed and representative results were chosen for analysis.
The Stanford Synchrotron Radiation Project, which opened to visiting researchers in 1974, used electromagnetic radiation generated by particles circling in SPEAR to explore samples at a molecular scale.
The Diagnostics & Genomics segment provides solutions that include reagents, instruments, software and consumables that enable customers in the clinical and life sciences research areas to interrogate samples at the molecular level.
In addition, gelatin zymography demonstrated the presence of gelatinolytic activities in all saliva samples at apparent molecular weights of 92 kD and 80 kD corresponding to latent and active MMP-9, respectively.
It is thus possible that checkpoint weakening in tumor samples at the molecular level is caused by altered activity of checkpoint components or by altered post-translational modifications that contribute to efficiency of the mitotic arrest.
Likewise, Py-GC/MS is also a widely used analytical tool to characterize recalcitrant macromolecules and polymeric samples at the molecular level [ 5, 15, 16].
Such studies could reveal differences and similarities between groups of samples at different molecular levels and provide a fundament for enhanced knowledge of the biological dynamics of breast cancers.
Molecular biological samples were stored at −20 °C and analyzed en masse at the end of the sampling program.
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