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The second set, termed genomic background probes, are based on probes designed to Genscan Suboptimal exon predictions (unlikely to be transcribed) from an old version of the human genome (NCBI Build 31).
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The majority of existing techniques to monitor hypertrophy in vitro are based on florescence probes designed to show morphological and biochemical alterations indicative of cardiomyocyte hypertrophy.
A quantitative real-time PCR (qPCR) detection method, based on a probe designed on B. cinerea intergenic spacer (IGS) regions and a reported probe for Vitis vinifera as internal control, was utilized to reveal the presence of symptomless infections on bunches.
The procedure is based on representative oligonucleotide probes designed by analyzing Bgl II restriction fragments of the human genome sequence.
The ROMA technology, invented at Cold Spring Harbor Laboratory and by NimbleGen [ 20], is based on representative oligonucleotide probes designed for fragments of the human genome sequence, which are more or less randomly distributed across the genome.
Colorimetric detection by gold nanoparticle probes was carried out using two 20-base thiolated probes designed based on the sequence of pta housekeeping gene of S. epidermidis.
Furthermore, in vivo cancer imaging techniques based on rationally designed activatable probes such as cancer-specific antibodies tagged with acidic-pH activatable fluorescence probes and peptidase activatable fluorescence probes were also discussed.
Development of c-Met targeting probes based on specifically designed peptides with high affinity and stability could help enhance diagnostic efficacy and therapeutic effects in c-Met positive cancers.
This implies development of new concepts for metal-speciation measurements in association with both voltammetric measurements and biogeochemical processes, new bioanalogical sensors, modern micro-total-analytical systems, and rugged submersible probes based on specifically designed mechanics, electronics and software.
NIR calibration models were developed and validated for the probe based on a designed 50-sample calibration set.
Objectives: Here we report a new real-time (LightCycler) quantitative PCR for the detection of HBV DNA based on sequence specific hybridisation probes (designed in-house), targeting the HBV surface antigen.
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