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Therefore, low concentration of target molecules can be captured and detected by this microarray.
In the absence of the target DNA sequence, the DLP maintains its hairpin structure in solution phase and would not be captured and detected by the β-CD/ACNTs electrode.
These capabilities allow large, micrometer-sized cell and particle trapping between the gratings, while smaller nanometer-sized proteins and analytes could be captured and detected within the pores.
Regardless of the fate of the specific microbe, its DNA can be captured and detected at the time of a metagenomic sampling.
These polyclonal fluids are used at high concentration to insure that all VLP antigens, even those with dramatically altered epitopes, should be captured and detected similarly.
Through formaldehyde cross-linking followed by proximity-based ligation, long-range chromosomal interactions can be captured and detected by PCR (chromatin conformation capture, 3C), microarray analysis or high-throughput sequencing (4C or 5C), with limited scale and selective bias [ 46- 48].
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Lipid rafts were captured and detected by the method we have previously used for detection of detergent isolated lipid rafts [ 23, 49].
Cytokines present in supernatants were captured and detected using appropriate antibody pairs (R and D Systems, Abingdon, UK) and a LabScan fluorescence plate reader.
The isolated lipid rafts were captured and detected with anti-Thy-1 and anti-Ly-6A.2 monoclonal antibodies respectively.
All positive controls exhibited the expected binding pattern and were captured and detected by their specific mAbs in the ELISA.
The DNA RNA hybrids were captured and detected by reporter molecule-labelled antibodies as described before (Sun et al, 2001).
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