Here, we directly characterized in vivo ribosome assembly intermediates and associated assembly factors from wild-type Escherichia coli cells using a general quantitative mass spectrometry (qMS) approach.
Microsomes were prepared form a mixture of 10 individual human liver samples (mixed on the basis of equal mass) using a general differential centrifugation procedure.
We tested the relationship of both DEA and mass-standardized DEA with soil variables and FD using a General Linear Model (GLM) with normal error distribution for each sample date.
The methyl eugenol was isolated from the serum using a general solid-phase extraction and was measured in the extract using gas chromatography/high-resolution mass spectrometry.
The continuity, momentum, and energy equations with mass and heat source/sink terms produced by chemical reactions are solved using a general computational fluid dynamic codes.
Differences in litter sizes were analysed using a general linear model (GLM) with pairing (P or NP male) as a fixed factor and female body mass as a covariate.
We tested for differences in body masses among treatments using repeated measures analysis of variance, and for differences in resting between pre- and post-flight period and among individuals and treatments using a general linear model.
In this study, a general mass transfer model for extraction with liquid surfactant membranes (LSMs) is proposed by using the operator theory.
We use a generalized law of mass action that is more general where both reaction parameters may be general nonlinear functions.
Monoisotopic mass values with an unrestricted protein mass using a peptide mass tolerance of ±100 ppm were used for identification.
