*<p>Restriction sites (underlined) introduced in primers: <u>GGTACC</u> (<i>Kpn</i>I), <u>GGATCC</u> (<i>Bam</i>HI), <u>ACTAGT</u> (<i>Spe</i>I), and <u>TCTAGA</u> (<i>Xba</i>I). Default PCR conditions were: initial denaturation, 95°C/5 min; denaturation, 94°C/30 s; number of cycles, 30; and final extension, 72°C/7 min.</p
<p>The restriction sites used were underlined.</p><p>Primers used in this study.</p
<p>#Restriction enzyme <i>Xma</i>I sites are in italics and underlined.</p>*<p>Point mutation sites ...
<p>The underlined sequence contains the restriction enzyme sites added for cloning purposes. Primers...
<p>Note: N = A, G, C or T; R = A or G; Y = C or T; M = A or C; S = G or C; K = G or T; V = A, C or G...
<p>All PCR primers shown here were designed for this study.</p>a<p>Restriction sites are underlined....
a<p>The underlined sequences are restriction enzyme sites: <i>Acc</i>65I sites (P1F and P7F), <i>Bam...
<p>Restriction site used in cloning is underlined.</p><p>Primers used in this study.</p
<p>(Restriction sites are underlined.)</p><p>Primers used for PCR amplification.</p
<p><sup><i>a</i></sup>Endonuclease restriction sites are underlined.</p><p><sup><i>b</i></sup>Restri...
<p>Predicted fragment sizes (approximate, in bp) and PCR cycle profiles (temperature in °C: time in ...
<p><sup>a</sup> Underlined nucleotides indicate the restriction enzyme sites.</p><p>Primers used in ...
<p>Restriction sites and T7 promoter sequences are underlined for the primer pairs used for cloning ...
a<p>Restriction sites are underlined; overlaps to other primers for PCR fusions are shown by lower c...
<p><sup>a</sup>Underlined nucleotides are restriction sites of the enzymes indicated in the brackets...
<p><sup>a</sup> Underlined sequences correspond to restriction enzyme sites introduced for cloning p...
<p>The restriction sites used were underlined.</p><p>Primers used in this study.</p
<p>#Restriction enzyme <i>Xma</i>I sites are in italics and underlined.</p>*<p>Point mutation sites ...
<p>The underlined sequence contains the restriction enzyme sites added for cloning purposes. Primers...
<p>Note: N = A, G, C or T; R = A or G; Y = C or T; M = A or C; S = G or C; K = G or T; V = A, C or G...
<p>All PCR primers shown here were designed for this study.</p>a<p>Restriction sites are underlined....
a<p>The underlined sequences are restriction enzyme sites: <i>Acc</i>65I sites (P1F and P7F), <i>Bam...
<p>Restriction site used in cloning is underlined.</p><p>Primers used in this study.</p
<p>(Restriction sites are underlined.)</p><p>Primers used for PCR amplification.</p
<p><sup><i>a</i></sup>Endonuclease restriction sites are underlined.</p><p><sup><i>b</i></sup>Restri...
<p>Predicted fragment sizes (approximate, in bp) and PCR cycle profiles (temperature in °C: time in ...
<p><sup>a</sup> Underlined nucleotides indicate the restriction enzyme sites.</p><p>Primers used in ...
<p>Restriction sites and T7 promoter sequences are underlined for the primer pairs used for cloning ...
a<p>Restriction sites are underlined; overlaps to other primers for PCR fusions are shown by lower c...
<p><sup>a</sup>Underlined nucleotides are restriction sites of the enzymes indicated in the brackets...
<p><sup>a</sup> Underlined sequences correspond to restriction enzyme sites introduced for cloning p...
<p>The restriction sites used were underlined.</p><p>Primers used in this study.</p
<p>#Restriction enzyme <i>Xma</i>I sites are in italics and underlined.</p>*<p>Point mutation sites ...
<p>The underlined sequence contains the restriction enzyme sites added for cloning purposes. Primers...