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Numerous alternative immunofluorescence-based protocols exist for the quantification of signaling events in cells.
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Real-time PCR (qPCR) is the principal technique for the quantification of pathogen biomass in host tissue, yet no generic methods exist for the determination of the limit of quantification (LOQ) and the limit of detection (LOD) in qPCR.
Several strategies exist for the metabolic labeling for the relative quantification of proteins, depending on the experimental system of interest.
Various writing systems exist for the language.
Estimates do exist for the three species.
Electrochemical detectors already exist for the job.
Several peripherals exist for the SG-1000 series.
In addition to protein arrays, other techniques exist for protein quantification, such as mass spectrometry (MS).
Although some semi-automated image processing methods exist for quantification of neurite outgrowth, methods to quantify axonal fasciculation in terms of direction of neurite outgrowth are lacking.
For example, fluorescence-activated cell sorting (FACS) protocols exist for quantification of events as diverse as apoptosis and immune signaling in a broad range of cell lines.
Although quantification of animal traits exists for the species studied here (Herrera 1984; Jordano 1987), our system is unfortunately too small (36 interactions) to support models with these additional explanatory variables.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com