Sentence examples for sequences for the amplification from inspiring English sources

Primers were designed such that they contained gene-specific sequences for the amplification of the respective ORFs.

Primer sequences for the amplification of GAPDH and TGF-β were selected from previously published sequences [ 53] (Table 2).

The primer sequences for the amplification of GAPDH were as follows: 5′-GCCAAAAGGGTCATCATCTC-3′ (forward); 5′-GGCATGGACTGTGGTCATGAG-3′ (reverse).

The sequences for the amplification of human PDGF-B were: 5′-TGTGGGCAGGGTTATTTAATATGG-3′ (forward) and 5′-CCATTGGCCGTCCGAATC-3′ (reverse).

See Additional file 3 for primer sequences for the amplification of the cDNA opsin genes in cichlids (RH2aα and RH2aβ combined).

Primer sequences for the amplification of Rf- and Rs-loci are given in Vargo [ 38] and Hayashi et al. [ 39], respectively.

The two contigs aligned to amplification boundary coordinates were selected as candidate breakpoint sequences for the SUL1 amplification and examined in detail.

Primer sequences used for the amplification are the same as described in previous publications [ 27– 31].

Primer sequences used for the amplification of rlukS-PV and rlukF-PV from the S. aureus MW2 DNA are presented in Table  1.

The sequences used for the amplification primers are as follows: Forward primer, TGCATCGCCCTCCTTGTG; Reverse primer, AGAAAGGCATGGAGAAAGAAGGTTT. Identification of the G allele was accomplished using the probe CACCACACACATGAT-8 labelled with VIC.

The primer sequences used for the amplification were 5′-TGTGAATTCGCCATGGGAGAGGC-3′ (forward) and 5′-TAACTCGAGCGTGCGGCGCCGCTT-3′ (reverse) for MRGBP, and 5′-ATAGAATTCTCTTCTGTCATGAGAAGTGG-3′ (forward) and 5′-ATACTCGAGTCACTTTTTCATCTTC-3′ (reverse) for BRD8.