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Banding patterns were obtained by random amplification of polymorphic DNA (RAPD), and specific D9S50 and D9S52 microsatellites (9p21).
LAB strains were typed by random amplification of polymorphic DNA-PCR (RAPD) typing with primers M13 (5′-GAGGGTGGCGGTTCT-3′) and LP1 (5′ACGCGCCCT-3′).
Toxicity measurement by Random Amplification of Polymorphic DNA (RAPD) technique revealed bivalve DNA banding pattern in treated Methyl Orange sample suggesting less toxic nature of phytotransformed dye products.
Sixty bacterial strains were encountered by random amplification of polymorphic DNA (RAPD) and repetitive extragenic palindromic (REP) typing in a series of 306 Lactococcus lactis isolates collected during the manufacturing and ripening stages of five traditional, starter-free cheeses made from raw milk.
Distinct clonal groups of E. coli were identified by Random Amplification of Polymorphic DNA (RAPD) and Multilocus sequence typing (MLST) from animals with uterine disease and these differed from known diarrhoeic or extra-intestinal pathogenic E. coli.
All three Rdg2a candidates were found to be transcribed in resistant embryos, and the transcript structures (Figure 2A) were determined by random amplification of cDNA ends (RACE) and RT-PCR.
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Further work can be done to confirm the role of V. hookeriana as the pollen parent of V. Miss Joaquim by using random amplification of polymorphic DNA.
Another gene from this cluster, sen, was only detectable by random amplification.
The sequences produced by random amplification and RPM version 1 were identical to those identified by the conventional sequencing method with the exception of ambiguous base calls (Ns).
Identification of H. capsulatum isolates was confirmed by using Polymerase chain reaction (PCR) was conducted with a probe from the M antigen, and the isolates were characterized by means of Random amplification of polymorphic DNA (RAPD -PCR employed the 1253 oligonucleotide and a mixtuRAPD -PCRgonuclemployed1281 and 1283.
Forty-eight strains of Listeria monocytogenes were genotyped by two rapid methods: random amplification of polymorphic DNA (RAPD) and 16S to 23S rRNA internal transcribed spacer fragment length polymorphism (ITS), and compared to the more time-consuming pulsed-field gel electrophoresis (PFGE).
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