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In this technique, known as the argon-40 argon-39 argon-40 argon-39 argon-40 argon-39n be determethodin the mass spectrometer as some of the potassium atoms in the sample are first converted to argon-39 in a nuclear reactor.
Residual drug levels present in a sample are first quantified by determination of FL expression, autocrine drug synthesis is then induced, and NAb activity is quantified from the difference in the ratio of FL/RL expression in the presence or absence of the sample.
For the prediction, mutations present in a sample are first translated into a 'transcriptomic fingerprint' by running ROC analysis on mutation and RNA-seq data.
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In this method, the seawater sample was first processed by removing nitrite and ammonium.
The sample was first allocated across 29 provinces, each of which was taken as a universe.
The sample is first excited with a low-incident power density equal to 70 W·cm−2.
Each sample was first sieved in wet conditions using a 3 − φ sieve.
Each sample was first weighed and then placed into a 5 ml test tube.
The sample was first stratified by geopolitical region.
Every DNA sample was first tested for DNA fragmentation by electrophoresis on a 1% agarose gel.
The sample was first analyzed on an LTQ Orbitrap equipped with the original HCD cell.
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