<p><b>A</b>. Effect of DNA dilution during ligation on iPCR amplification of staggered-end fragments from HsInv0340 of 32 kb (AB) and 40 kb (BD) and the A–D concatamer. <b>B</b>. Effect of different reagent concentrations during ligation on iPCR amplification of blunt-end fragments from HsInv0286 of 33 kb (BD) and 41 kb (AB). The A–D fragment with 10 ng/µl of DNA and the 41 kb fragment with no additional reagent were selected as reference to calculate the relative amplification in <b>A</b> and <b>B</b>, respectively. NA18517 DNA that is heterozygous for both inversions was used in the analysis.</p
<p>Standard curves were generated by qPCR using as template 5-fold serial dilutions of heteroplasmic...
DNA adducts are covalent modifications to DNA strands that includes strand breaking, cross linking a...
*<p> <i>Vector and donor beads were loaded at 0.5 ng DNA/µg bead.</i></p
<p>(A) Primers used to amplify the <i>Hbb-b1</i> promoter–HS4/5 ligation junction. (B) Primers to an...
DNA amplification is a very powerful tool that can be used to replicate one molecule of DNA into mil...
<p><b><b><i>A</i></b><b>.</b></b> Test of pLib2 vector self-ligation alone (lane 2) or in the presen...
This work presents a novel method for detecting nucleic acid targets using a ligation step along wit...
Mixed CRV and CEV plasmids were diluted as templates from 1×105 to 1×103 copies/μl to amplify specif...
<p><b>A</b>. HsInv0403 ABD and ACD iPCRs. Band sizes are: AB, 364 bp; BD, 239 bp; AC, 350 bp; CD, 22...
The ability to obtain deoxyribonucleic acid (DNA) profiles is generally considered a powerful tool w...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
<p>The DNA of each H37Rv:XDR-TB mixture was diluted 10 fold serially and subjected to real-time PCR ...
The rate of amplification of abundant PCR products generally declines faster than that of less abund...
<p>PalB/PalA or HIV38A/HIV38B duplexes (12.5 nM) were incubated with increasing concentrations of IN...
<p>Bar graphs depict the fraction of either ligated DNA (product, blue) or abortive adenylylation (A...
<p>Standard curves were generated by qPCR using as template 5-fold serial dilutions of heteroplasmic...
DNA adducts are covalent modifications to DNA strands that includes strand breaking, cross linking a...
*<p> <i>Vector and donor beads were loaded at 0.5 ng DNA/µg bead.</i></p
<p>(A) Primers used to amplify the <i>Hbb-b1</i> promoter–HS4/5 ligation junction. (B) Primers to an...
DNA amplification is a very powerful tool that can be used to replicate one molecule of DNA into mil...
<p><b><b><i>A</i></b><b>.</b></b> Test of pLib2 vector self-ligation alone (lane 2) or in the presen...
This work presents a novel method for detecting nucleic acid targets using a ligation step along wit...
Mixed CRV and CEV plasmids were diluted as templates from 1×105 to 1×103 copies/μl to amplify specif...
<p><b>A</b>. HsInv0403 ABD and ACD iPCRs. Band sizes are: AB, 364 bp; BD, 239 bp; AC, 350 bp; CD, 22...
The ability to obtain deoxyribonucleic acid (DNA) profiles is generally considered a powerful tool w...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
<p>The DNA of each H37Rv:XDR-TB mixture was diluted 10 fold serially and subjected to real-time PCR ...
The rate of amplification of abundant PCR products generally declines faster than that of less abund...
<p>PalB/PalA or HIV38A/HIV38B duplexes (12.5 nM) were incubated with increasing concentrations of IN...
<p>Bar graphs depict the fraction of either ligated DNA (product, blue) or abortive adenylylation (A...
<p>Standard curves were generated by qPCR using as template 5-fold serial dilutions of heteroplasmic...
DNA adducts are covalent modifications to DNA strands that includes strand breaking, cross linking a...
*<p> <i>Vector and donor beads were loaded at 0.5 ng DNA/µg bead.</i></p