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In a six-compartment EH cell, a recovered acid concentration of 50 g/L can be obtained in 12 h operation at 45 °C and a cell current density of 225 A/m2 with a cell voltage of 5.9 6.5 V.
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Two lab-scale electrohydrolysis (EH) cells have been used to study the effectiveness of this method in the recovery of sulphuric acid from copper-containing electrolytes such as those present in copper electrorefining.
DIMM cells already known to display this property include the Inka cells [73], EH cells [7], and Bursicon/CCAP cells [11].
The first cells to respond are the DIMM-positive Tv neurons (expressing dFMRFa), followed by the EH cells, then DIMM-positive CCAP cells (cell 27/703), and finally the DIMM-positive Bursicon/CCAP-containing of the abdominal segments.
These results were also consistent with changes in Eh and cell densities.
MicrRNA-135a-5p MicrRNA-135a-5p MicrRNA-135a-5p MicrRNA-135a-5pion and colony formimicn abilitransfection and EH-GB1 could (Finhibit,c), and arresthehe cells in G1/S proliferation3and
Glutathione S-transferases (GSTs) and epoxide hydrolases (EHs) protect cells from exogenous insult by detoxifying electrophilic compounds.
Both GBC-SD and EH-GB1 cells were infected with recombinant lentivirus plus 6 μg/mL polybrene (Sigma Aldrich).
In both GBC-SD and EH-GB1 cells, VLDLR could reduce the phosphorylation level of p38 (Figs 4c,S4c), and we also found that VLDLR-siRNA could induce phosphorylation of p38 (Fig. S4c).
Potential targets of miR-135a-5p miR-135a-5p miR-135a-5ptScan (http://weretargetscan.org) and predictedttp://pictar.mdc-byrlin.de), and mRNA microarray assays were carried ouTargetScan1 cells transfected withttpR-135a-5p mimic.
We then established stable GBC-SD and EH-GB1 cells overexpressing miR-135a via lentivirus (Fig. S2d), and found that the proliferation rates of lenti-miR-135a GBC cells were significantly decreased compared with those cells infected with lenti-GFP (Fig. 2a,b).
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