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The result is a pattern of blue lines on a nylon strip, which is visually read by comparing the pattern with a reference guide.
Plasma samples were tested for HIV/SIV antibodies by the INNO-LIA HIV Confirmation test (Innogenetics, Ghent, Belgium), which includes HIV-1 and HIV-2 recombinant proteins and synthetic peptides that are coated as discrete lines on a nylon strip.
The INNO-LIA syphilis score is based on the enzyme immunoassay principle in which TpN47, TpN17, and TpN15 recombinant proteins and TmpA synthetic peptide are coated as discrete lines onto a nylon strip with plastic backing.
The Inno-Lia is a WB-like line immunoassay that measures antibodies against recombinant proteins or synthetic peptides of HIV-1 group M, HIV-1 group O, or HIV-2, which are coated as 7 discrete lines on a nylon strip.
The Inno-Lia is a Western blot-like line immunoassay that measures antibodies against recombinant proteins or synthetic peptides of HIV-1 group M, HIV-1 group O, or HIV-2, which are coated as 7 discrete lines on a nylon strip with plastic backing.
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One man breezily glided his hand over the nylon strip, tied tight across four columns by the track for Manhattan-bound trains.
(Or wrap the nylon strip in same direction as the wire) Place the wire (Or strip of nylon) around the vine (A) when it is under the trellis wire (B).
The blend and its variant were dispensed using nylon strips inserted in the attractant plume tube of an MM-X® trap (a counter flow geometry trap made by American Biophysics Corporation) and CO2 gas was added to the trap using rubber tubing (Figs. S1-S3).
Then, HPV-DNA amplicons were chemically denatured to single-stranded DNA, hybridised with matching type-specific DNA probes, immobilized on nylon strips, and detected by colorimetric determination.
In a reverse-line blot assay, 40 μL of the denatured product were added to 3 mL of hybridization buffer containing the HPV genotypes and 2 concentrations of the β-globin probes, immobilized on nylon strips.
The method includes a PCR amplification of extracted HPV DNA using a pool of biotinylated primers that hybridise in the L1 region of the HPV genome, chemical denaturation of HPV DNA amplicons to single-stranded DNA, followed by hybridisation with matching type-specific DNA probes immobilised on nylon strips, and detection by colorimetric determination.
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