<p>*The T7 promoter regions are underlined and the restriction enzyme sites are italicized.</p
<p>Primers that have been used to generate GFP- miRNA target gene constructs. Restriction sites are ...
<p>*Restriction sites are in bold; primer regions that anneal to 2A<sup>pro</sup> gene are underline...
<p>(Restriction sites are underlined.)</p><p>Primers used for PCR amplification.</p
<p>Primers used for making CYP2E1 promoter luciferase reporter gene constructs.</p
a<p>Nucleotides in bold indicate restriction sites introduced for cloning.</p>b<p>T7 RNA polymerase ...
<p>Restriction sites and T7 promoter sequences are underlined for the primer pairs used for cloning ...
<p>The mutations introduced into the binding sites are italicized and in lowercase.</p><p>Primers us...
<p>T7 promoter (not shown) was added to the 5′ end of each primer for in vitro transcription of dsRN...
<p>*The restriction enzyme sequence is underlined.</p><p>**T7 promoter sequence is in bold.</p
<p>These plasmids were verified by DNA sequencing. Underlined nucleotides indicate the designated si...
<p>C2-A, C2-B, C2-C, C2-D, C2-E, C2-a, C2-b, C2-c and C2-d: Forward primers for construction of the ...
<p>Primers starting with a D were degenerated primers to get the partial CDS of each gene. Primers s...
<p>Restriction enzyme sites are underlined.</p><p>Additional nucleotides added to facilitate restric...
<p><sup>a</sup> Underlined nucleotides indicate the restriction enzyme sites.</p><p>Primers used in ...
<p>Restriction enzyme sites generated by site-directed mutagenesis or by PCR are boldfaced and under...
<p>Primers that have been used to generate GFP- miRNA target gene constructs. Restriction sites are ...
<p>*Restriction sites are in bold; primer regions that anneal to 2A<sup>pro</sup> gene are underline...
<p>(Restriction sites are underlined.)</p><p>Primers used for PCR amplification.</p
<p>Primers used for making CYP2E1 promoter luciferase reporter gene constructs.</p
a<p>Nucleotides in bold indicate restriction sites introduced for cloning.</p>b<p>T7 RNA polymerase ...
<p>Restriction sites and T7 promoter sequences are underlined for the primer pairs used for cloning ...
<p>The mutations introduced into the binding sites are italicized and in lowercase.</p><p>Primers us...
<p>T7 promoter (not shown) was added to the 5′ end of each primer for in vitro transcription of dsRN...
<p>*The restriction enzyme sequence is underlined.</p><p>**T7 promoter sequence is in bold.</p
<p>These plasmids were verified by DNA sequencing. Underlined nucleotides indicate the designated si...
<p>C2-A, C2-B, C2-C, C2-D, C2-E, C2-a, C2-b, C2-c and C2-d: Forward primers for construction of the ...
<p>Primers starting with a D were degenerated primers to get the partial CDS of each gene. Primers s...
<p>Restriction enzyme sites are underlined.</p><p>Additional nucleotides added to facilitate restric...
<p><sup>a</sup> Underlined nucleotides indicate the restriction enzyme sites.</p><p>Primers used in ...
<p>Restriction enzyme sites generated by site-directed mutagenesis or by PCR are boldfaced and under...
<p>Primers that have been used to generate GFP- miRNA target gene constructs. Restriction sites are ...
<p>*Restriction sites are in bold; primer regions that anneal to 2A<sup>pro</sup> gene are underline...
<p>(Restriction sites are underlined.)</p><p>Primers used for PCR amplification.</p
DOI
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