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Exact(25)
Brain samples were homogenized using a Virsonic 100 ultrasonic homogenizer.
The brain samples were homogenized in ceramic mortars by using sterile quartz sand, and the homogenates were suspended in RNase-free distilled water.
The brain samples were homogenized together in ice-cooled CH3CN/H2O (1.0, 1.0 mL) solution using the Silent Crusher S (Heidolph Instruments, Schwabach, Germany).
Briefly, cultured cells or brain samples were homogenized in supplied buffers.
Aliquots of brain samples were homogenized and extracted in 0.2% diethylamine (DEA)/50 mM NaCl at 1∶10 W/v.
Briefly, brain samples were homogenized using the stainless steel beads before using the RNeasy Plus Mini kit.
Similar(35)
Briefly, brain tissue samples were homogenized in 2∶1 chloroform:methanol containing 0.5% butylated hydroxytolulene and lipids were extracted by the method of Folch [58].
Frozen brain tissue samples were homogenized on ice using ultrasound in a 3-fold (w/v) volume of 1% (w/v) sulfosalicylic acid.
The frozen brain tissue samples were homogenized in 0.3 M perchloric acid (1 mg : 6 μL).
After weighing, the brain tissue samples were homogenized with 1 mL of saline at 10,000 rpm for 1 min over ice using a tissue homogenizer (Kinematica, Switzerland).
For brain IP, samples were homogenized in LB (2.5 mg tissue per 1 ml of buffer), using a Potter-type homogenizer, pulsed by sonication (15 s, two pulses) and cleared by centrifugation (4°C, 17 000 g, 30 min).
More suggestions(16)
brain samples were examined
brain samples were postfixed
brain microvessels were homogenized
brain samples were placed
brain sections were homogenized
brain samples were fixed
brain samples were isolated
brain samples were cleared
brain samples were deproteinized
brain parts were homogenized
brain samples were measured
brain samples were included
brain samples were weighed
brain samples were performed
brain samples were set
brain samples were thawed
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