Example sentences of "[vb pp] at [num] g " in BNC.
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1 | Homogenates were centrigued at 40000 g for 90 minutes at 4°C , and the pellet was resuspended in homogenisation buffer . |
2 | The samples were immediately ultracentrifuged at 100000 g for two hours at 37°C ( Hitachi 55P-72 , Tokyo , Japan ) . |
3 | The thawed samples were spun at 1000 g for 10 minutes and 500 µl aliquots were taken into a second acid washed plastic tube , diluted 1:9 with ultrapure 0.11 M nitric acid , and analysed by ICPES ( Philips PV 8050 ) at the following wavelengths : potassium 766.49 nm , sodium 588.99 nm , magnesium 383.83 nm , copper 324.75 nm , calcium 315.89 nm , iron 259.94 nm , and zinc 213.86 nm . |
4 | ( iii ) Centrifuge the cell suspension obtained at 50 g for 5 min . |
5 | Oral acyclovir has been maintained at 4 g orally per day . |
6 | Cell suspensions were centrifuged at 200 g for 10 minutes and the pellet of cells added to the organ bath the bathing fluid of which was used to resuspend them for transfer . |
7 | The homogenates were centrifuged at 3000 g for 15 minuts . |
8 | To minimise loss of APGPR immunoreactivity on storage , each urine sample was centrifuged at 3000 g for 20 minutes , the supernatant suspended in a boiling bath for 10 minutes , centrifuged for five minutes at 10000 g , and the supernatant aliquoted and stored at -20°C until assayed . |
9 | This pooled concentrated urine was then centrifuged at 10000 g for five minutes and 1 ml of supernatant chromatographed on a Sephadex G-25 column ( 0.9×43 cm ) in TRIS buffered saline ( TBS ) containing 50 mM TRIS/HCl , 0.15 M NaCl , 3.1 mM NaN 3 at pH 7.3 at a flow rate of 39.5 ml/ hour and 1.056 ml fractions collected and assayed using the APGPR ELISA . |
10 | After sonication , the sample was centrifuged at 150000 g for one hour to yield a faintly opalescent supernatant consisting of a homogeneous population of cholesteryl oleate vesicles . |
11 | Each tube was centrifuged at 1500 g for 10 minutes and after separation , the radioactivity of the pellet was counted in an LKB 1271 RIAGAMA counter ( Turku , Finland ) . |
12 | Twenty millilitres were centrifuged at 1500 g for 10 minutes to obtain cell free plasma . |
13 | This suspension was centrifuged at 1500 g for 10 minutes . |
14 | The resulting crude homogenate was then centrifuged at 600 g for 10 minutes to remove unbroken cells and nuclear debris . |
15 | The filtered solution was then centrifuged at 3 g for 5 minutes , the supernatant removed , and the cells resuspended in 10 ml of HBSS solution . |
16 | Biopsy homogenates were centrifuged at 7000 g for 15 minutes at 4°C and the pellets resuspended in the homgenisation buffer to obtain a protein concentration of 1–4 mg/ml . |
17 | The solution was centrifuged at 1700 g for 30 minutes at 4°C . |
18 | The sonicated samples were centrifuged at 20000 g for 20 minutes and the supernatants were stored frozen at -80°C until assay . |
19 | After incubation , tubes were centrifuged at 1000 g and the supernatant separated from the pellet . |
20 | The solution was centrifuged at 1000 g for 10 minutes , the supernatant was discarded and 1.5 µCi/kg body weight of disodium ( 51 ) chromate was added dropwise to the pellet of red cells while mixing gently . |
21 | The reaction was stopped by the addition of 11 N HCLO 4 and the cells were centrifuged at 4000 g , 10 minutes . |
22 | Tubes were centrifuged at 17000 g for five minutes and the supernatants were recovered . |