%0 Generic %A Yu, Zhiliang %A Wang, Ju %A Lin, Jianxun %A Zhao, Minyan %A Qiu, Juanping %D 2015 %T Primers used in high-efficiency thermal asymmetric interlaced PCR. %U https://plos.figshare.com/articles/dataset/_Primers_used_in_high_efficiency_thermal_asymmetric_interlaced_PCR_/1359464 %R 10.1371/journal.pone.0122741.t004 %2 https://ndownloader.figshare.com/files/1993289 %K rf %K lao gene expression %K Desired transposon insertion %K LAAO production %K GntR family transcriptional regulator %K gcn %K LAAO activity %K marine bacterium Pseudoalteromonas sp %K mutant %K Exploring Regulation Genes %K role %K Pseudoalteromonas sp %X

a DTn10AP1, DTn10AP2 and DTn10AP3 are primers specific to transposon gene and were used to retrieve the disrupted genes in mutants; LAD1-1, LAD1-2, LAD1-3, LAD1-4 and LAD1-5 are arbitrary primers which were designed based on the report [27]; the remaining primers were designed based on the intermediate sequences of the disrupted genes in mutants B1, B6 and B19, respectively, and used to amplify for 3’-region of sdmT gene (Fsdmt1 (1st), Fsdmt2 (2nd), Fsdmt3 (3rd)), 5’-region of nhaD gene (RnhaD1 (1st), RnhaD2 (2nd), RnhaD3 (3rd)), 3’-region of nhaD gene (FnhaD1 (1st), FnhaD2 (2nd), FnhaD3 (3rd)), 5’-region of karI gene (Rkari1 (1st), Rkari2 (2nd), Rkari3 (3rd)), and 3’-region of karI gene (Fkari1 (1st), Fkari2 (2nd), Fkari3 (3rd)).

b V = A/C/G; N = A/C/G/T; B = C/G/T; H = A/C/T; D = A/G/T.

Primers used in high-efficiency thermal asymmetric interlaced PCR.

%I PLOS ONE