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Immediately after, one half of the animals (saline pre-treatment group, 11 26 per group) received another saline injection, and the other half was injected with AMPH (2 mg/kg, i.p).; locomotor activity was monitored for an additional 90 minutes.
A solution of 14 to 46 MBq of Tc-99m in less than 1 cc of water was prepared and approximately half was injected into each of the two empty syringes.
Within each of these groups, at feeding time (0800 h), half of the calves received an i.v. injection of naloxone (NAL, an opioid receptor antagonist; 1 mg/kg of BW) and the other half was injected with saline solution (SAL; 0.9% NaCl).
A 9 1 dilution of sample and 5% acid sulfanilamide (AS) was incubated for 5min; half was injected into the NOA (I 3 - assay) to give combined SNOHb and HbNO levels.
The other half was injected on the F4 to remove proteins binding with fast exchange kinetics, that is, the soft corona; leaving only proteins bound with slow exchange kinetics, i.e. the hard corona, to be coisolated with the SPIONs by F4.
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The second factor was that at approximately 7 d before expected calving date, half the cows in each feed group were injected with pegbovigrastim and the remaining half were injected with saline.
To study whether there are any side-effects in the days following a vaccination, US researchers vaccinated two thousand people, but only half were given the real vaccine, while the other half were injected with harmless salt water.
At day 1, half of the males in each group were intraperitoneally injected with a solution of lipopolysaccharides (LPS) from Escherichia coli (serotype 055 B5, Sigma) at a dose of 0.05 mg/kg, whereas the other half were injected with a phosphate buffered solution (PBS) for control.
Briefly, half of the rats were injected subcutaneously with 150 μL of pristane, and the other half were injected with normal saline (NS).
Among the mice that underwent surgical DMM, half were injected with FlammaTM675-ApoPep-1 FlammaTM675-ApoPep-1 FlammaTM675-ApoPep-1M675-NSSSVDK (control peptide; Bioacts) through the tand vein (100 nmol/20 g body weighthe(n = 8/grother
Each dose (1 mgm100 gm body wt) was divided equally into half (0.5 mgm100 gm body wt), and each half dose was injected twice daily (11 a.m. and 5 p.m).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com