Sentence examples for bp and a second from inspiring English sources

PEPCK fragments included a 173-bp exon, a length-variable intron (162 202 bp), and a second 183-bp exon.

For multiplex sequencing, DNA samples, each with a different barcode, are pooled, randomly sheared, size selected (300 700 bp), and a second adapter is ligated after polishing and filling ends.

A long PCR amplification generated a fragment of ~12,000 base pairs (bp) and a second reaction targeted a fragment of ~4,500 bp.

From profiles that presented near-even smears we excised two sets of amplification products, one covering a size range from 300 to 700 bp and a second one from 700 to 1500 bp.

Two genome-wide data-sets are considered, one including only those genomic regions for which all taxa are represented, which included 3,361,015 aligned nucleotide base-pairs (bp) and a second that additionally includes those regions present in only subsets of taxa, which totaled 12,456,624 aligned bp.

Other than these, the list contains one additional ATC tandem motif with an 8 bp spacer at the preferred location in RPL15 and one tri-partite tandem motif with the first spacer of 7 bp and a second one of 6 bp in RPS10.

wyomingensis individuals were multiplexed in approximately equal concentrations and sequenced in two separate runs (one single end 80 bp run, and a second paired end 80 bp run) on the Illumina Genome Analyzer at the Oregon State University Center for Gene Research and Biocomputing, Corvallis, OR.

In addition, we found duplicate paralogs of the Fzd8 gene based on 1,575 bp, extending the single known paddlefish (GB DQ307742.1) sequence by 150 bp and adding a second paralog sequence.

There were multiple sets of primers used for the analysis of the multicopy IS6110 target region: one PCR which used IS6110 primers [32] for a slightly longer target of 246 bp; another set of primers [33] that amplify a 123 bp product and a third set used in conjunction with the former for a nested PCR [20] which give a 92 bp product.

Initial conventional PCR assays employed a forward primer in the ND3 gene (upstream of ψND5-2) and a reverse primer in ND5 sequences downstream of the heteroplasmic deletion – genomic DNA samples from most global superclade C. briggsae isolates yielded one or two PCR products, one being ~1700 bp (intact genomes) and a second that is ~800 bp (deletion-bearing genomes) – see Figure 3A.

Amplified products for VP4 (663 bp) and VP7 (880 bp) were purified a second time using XTerminator™ and SAM™ solutions (Applied Biosystems™ Foster City, CA, USA).