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Gene expression analysis was performed using a Mouse Multiple Sclerosis RT² Profiler PCR Array, and further determinations and validations of the identified genes were performed using qPCR.
The conversion efficiency of the FF-DSSC based on a TiCl4-treated TiO2 nanorod array (hierarchical structure I) exhibits about 4 times higher than that based on a HCl-treated TiO2 nanorod array, and further rises to 4.4% when the TiCl4-treated TiO2 nanorod array is treated in a mixed solution of (NH4 2TiF6 and H3BO3 three times (hierarchical structure II).
It is used in the proposed system to create a buffer of a given size and continuously perform read and write process and store the buffer size for every second in an array and further perform analysis on this array for predicting the buffer capacity using our algorithm.
The array data were normalized to the 50th percentile of all genes detected to be present on the array and further normalized to the mean of specific samples depending on the comparison e.g. H37Rv in broth versus H37Ra in broth.
Differential expression of apoptosis-related genes was determined by gene array and further evaluated by Western blot analysis.
For each sample, 100 ng total RNA was hybridized with the miRNA array and further processed according to Agilent's miRNA Microarray System protocol.
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This chapter mainly discusses recent advances made in general assembly strategies for rational organization of semiconductor nanowires into well-ordered arrays and further integrating these architectures to functional devices.
A total of 101 defect arrays and further 801 duplicates of microarrays were removed.
Robust Multichip Analysis was used to normalise the different arrays, and further analysis was carried out with GeneSpring GX10 (version 11.5.1, Agilent Technologies, Inc., Tokyo, Japan).
Furthermore, the method exploits the identical geometry of the array elements and further reduces the memory requirement and CPU time.
Next, these FP CNVs were compared to the exaCGH array design and further analyzed.
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