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No experiments have been conducted on humans, but the inventor says that in laboratory tissue tests, the antibody stops this migration.
Information about mortality patterns, disease, and levels of environmental contaminants has been obtained from beached and stranded marine mammals, from studies designed to address these issues in wild populations, or from laboratory tissue studies.
In our laboratory, tissue culture techniques have been used successfully for propagation of several medicinally important plant species (Tsay [1999]; Nalawade et al. [2003]; Mulabagal and Tsay [2004]; Tsay and Agrawal [2005]; Chen et al. [2006] and Chang et al. [2007]).
In the laboratory, tissue was washed three times in warmed PBS, cut into approximately 2 cm2 pieces and placed (luminal side upwards) onto pieces of metal gauze within central-well tissue culture dishes containing warmed R5 media with nalidixic acid 50 mg/L.
After 24 h, the droplets were removed with a laboratory tissue.
We utilized laboratory tissue phantoms in order to assess the performance of both DCA-L1 and DCA-L2 regularizations.
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Between samples, the electrode was rinsed with 10% v/v HNO3 and Milli-Q water (R>18 MΩ cm. total organic carbon<2 μg C L-1) and gently blotted with <span class="lh">laboratory tissues.
In the laboratory, tissues were lyophilized prior to RNA extraction following [ 43].
In the laboratory, tissues were homogenized and total RNA was isolated using Trizol (Invitrogen, Carlsbad, CA) and subsequently cleaned using a Qiagen RNeasy column.
We found that DFI was effective and robust for selecting differential gene features for RNA-Seq experiments from different laboratories, tissue types, and cell origins.
In this study, we demonstrated that DFI can efficiently handle multiple groups of data simultaneously, and identify differential gene features for RNA-Seq experiments from different laboratories, tissue types, and cell origins, and is robust to extreme values of gene expression, size of the datasets and gene length.
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