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The method detection limit for EDXRF measurement was 6 30 ng using a 2 cm × 2 cm sorbent.
Here, we demonstrate enhancement of the output power of one-dimensional zinc oxide (ZnO) nanowires (NWs -based NWs -based p-type semicoNGusing polymer, by controlling their energy band at depletion width in the piezoelectric semiconductorg polymerction interface and native defects presented in as-grown ZnO NWs.
Antiadalimumab levels were expressed in arbitrary units (AU; 1 AU ≈ 12 ng) using a serum containing antiadalimumab as standard.
Polymerase chain reactions (PCR) were carried out on genomic DNA (10 ng) using a TaqMan universal PCR master mix (Applied Biosystems).
First-strand cDNA was synthesized from total RNA (1000 ng) using a High Capacity RNA-to-cDNA Kit (Applied Biosystems, Foster City, CA, USA).
RNA concentrations were determined using a Nanodrop ND-2000 spectrophotometer (Nanodrop Technologies, Wilmington, DE, U.S ., and the complementary DNA (cDNA) was synthesized from the total RNA (500 ng) using a PrimeScript® RT Reagent Kit (DRR037S, Takara Biotechnology, Dalian, China) in accordance with the manufacturer's instructions.
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The gas liquid equilibrium data for desulfuration of natural gas (NG) by using a mixed aqueous alkanolamine solution was investigated and the results were used for evaluating their ability of removing hydrogen sulfide.
Embryos at the one- to four-cell stage were injected with an abca12 morpholino (MO1, 25.6 ng) or snap29 morpholinos (MO2, 2.6 ng and MO3, 5.2 ng) using glass microelectrodes fitted to a gas pressure injector PL1-1000, Harvard Apparatus).
End-point PCR reactions were run on 50 100 ng cDNA using a HotStartTaq® polymerase (Qiagen).
Expression of WT and Kv7.1 mutants was performed by injecting 40 nl per oocyte (5 ng cRNA) using a Nanoject injector (Drummond, USA).
Amplifications were optimized in 50 μl reaction volumes containing about 50 ng cDNA using a PrimeScript RT-PCR Kit (Takara, Otsu, Japan).
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