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Fluorescently labeled cDNAs were generated from 20 μg of total RNA in each reaction using the Agilent Fluorescent Direct Label Kit and 1.0 mM Cyanine 3- or 5-labeled dCTP (PerkinElmer, Boston, MA), and following user's manual.
Twenty micrograms of total RNA were used to generate fluorescent Cy-3-labeled cRNA (control cells) and Cy-5-labeled cRNA (treated cells) using an Agilent Fluorescent Direct Label Kit.
Per microarray, 20 μg mRNA, pooled from 2 livers, was reverse transcribed with Cy3-labelled dCTP (Perkin Elmer, Boston, USA), using the Agilent Fluorescent Direct Label Kit.
500 ng of mRNA from tumors with high COX-2 patients was labeled with Cy-3-dCTP (Amersham BioSciences) in a cDNA synthesis reaction with Agilent Flourescent Direct Label.
The probe bears a direct label (e.g. fluorescein) or a tag for subsequent detection (e.g. biotin).
Total RNA (20 μg) was labeled using a Fluorescent Direct Label Kit (Agilent Technologies) and simultaneously reverse transcribed into cDNA.
Similar(46)
cDNA fluorescence-labeled probes were obtained by the direct labeling procedure in the presence of modified cy-3 and cy5 dCTP (Perkin Elmer) [51].
Devices may be used as a transducer for direct label-free biosensor development.
This constitutes a direct, label-free and signal-on electrochemical immunosensor, with a very low detection limit of ca. 1 pM, i.e. 0.2 ng L−1, one of the lowest reported for such immunosensors.
A direct, label-free immunosensor was designed for the rapid detection and quantification of staphylococcal enterotoxin A (SEA) in buffered solutions using quartz crystal microbalance with dissipation (QCM-D) as transduction method.
Both the drug loaded and unloaded formulations were labeled with 99mTc by the direct labeling method.
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