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About 50 μl of peripheral blood was collected from the caudal vein of the specimens on each sampling time using heparinized 1-ml disposable syringes and transferred to 1-ml eppendorf tube containing 450 μl of chilled Ca++- and Mg++- free phosphate buffer saline.
5 × 106 cells (2 mock-transfected clones, pUSE-9 and pUSE-12; and 2 activated MEK1-transfected clones, H-MEK1-15 and H-MEK1-17) were suspended in calcium free phosphate buffer saline and subcutaneously injected on both sides of the SCID mice.
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Tissue samples were collected in a sterile 15-ml centrifuge tube containing 1 ml of calcium and magnesium free phosphate buffered saline (PBS).
Following 3 hours of growth, the bacteria were pelleted at 5,900 g for 6 minutes and then washed two times with endotoxin free phosphate buffered saline (PBS).
Isolated islets were dissociated into single cell suspensions by careful pipeting after washing in 2 mM EDTA/PBS, and incubation for 10 min at room temperature in Ca2+ free phosphate buffered saline (PBS) supplemented with 0.025% trypsin.
For single cell studies of mitochondrial ATP levels, the islets were dispersed by incubation in Ca2+/Mg2+ free phosphate buffered saline, 3 mM EGTA and 0.002% trypsin as previously described [42].
and washed in cation free phosphate buffered saline (PBS).
To further explore the flat-band voltage drift effect and to challenge the assumption that alkali ions are involved in the drift we conceived a novel alkali-free phosphate buffer saline (AF-PBS) where the sodium and potassium ions are replaced by ammonium ion and tested the capacitor under similar conditions to standard PBS.
with 4×LD50 (4×104 p.f.u./ml) of PR8 virus (H1N1) in endotoxin-free phosphate buffer saline (PBS) under isofluran anaesthesia.
The cells were then washed three times with probe-free phosphate buffer.
Samples weighing approximately 1 g were dissected, rinsed in RNAase-free phosphate buffer, snap-frozen in liquid nitrogen and stored at -80°C.
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