Sentence examples for mer in length from inspiring English sources

An antisense oligonucleotide is preferably between 15 and 30 mer in length and specifically hybridizes with an mRNA around the translation start codon (Uhlmann and Peyman [1990]; Good et al. [2001]).

We identified 1511 non-redundant mononucleotide cMS repeats ≥7 mer in length (including hypothetical genes) predicted to generate NMD-resistant mutant transcripts.

We limited the study to the 316 mononucleotide cMS repeats ≥8 mer in length, since there is a correlation between microsatellite length and likely mutation frequency.

Probe sizes were 50 75 mer in length and median probe spacing was 200 bp.

The probe size ranged from 50 to 75 mer in length with median probe spacing of 1,395 bp.

Peptide nucleic acid clamp primers, 14- to 18- mer in length, were designed according to the guidelines (Ugozzoli et al, 2004).

Two strands of synthetic oligonucleotides used here were designed with 50-mer in length and the sequences are semi-complimentary so to hybridize spontaneously into concatemers of double stranded DNA.

Both strands of the total of 1,599 mRNA sequences were doubly represented by a total of 334,372 oligo DNA probes 50-mer in length, with no gap between the probes (Figure 1).

In order to detect these fragments, we adopted a tiling array strategy for the design of custom oligo DNA microarrays as follows: 1) Oligonucleotide probes of 50-mer in length were used.

To manufacture ORF-specific DNA microarrays, approximately 10,000 oligonucleotides (50-mer in length) that represented 4,929 ORFs (one ORF is represented by two oligomers) in the S. pombe genome [32] were synthesized (Proligo, Hamburg, Germany).

We constructed transcription-factor tiling (TFT) arrays containing ∼1,600 open reading frame sequences of known and predicted mouse transcription-regulatory factors (334,372 oligonucleotides, 50-mer in length) to analyze cDNA fragments from mRNA-display screening for Jun-associated proteins.