<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-2768</journal-id>
<journal-title><![CDATA[Polibotánica]]></journal-title>
<abbrev-journal-title><![CDATA[Polibotánica]]></abbrev-journal-title>
<issn>1405-2768</issn>
<publisher>
<publisher-name><![CDATA[Instituto Politécnico Nacional, Escuela Nacional de Ciencias Biológicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-27682026000100205</article-id>
<article-id pub-id-type="doi">10.18387/polibotanica.61.12</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Improvements to a commercial DNA extraction method for high-quality nucleic acid extractions from Populus tremuloides Michx. vegetative buds]]></article-title>
<article-title xml:lang="es"><![CDATA[Mejoras en un método comercial de extracción de ADN para obtener extractos de ácido nucleico de alta calidad a partir de yemas vegetativas de Populus tremuloides Michx.]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gutiérrez-Contreras]]></surname>
<given-names><![CDATA[Cecilia Nataly]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Barraza-Salas]]></surname>
<given-names><![CDATA[Marcelo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mercedes Porth]]></surname>
<given-names><![CDATA[Ilga]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Wehenkel]]></surname>
<given-names><![CDATA[Christian]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Juárez del Estado de Durango  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Juárez del Estado de Durango Facultad de Ciencias Químicas ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Université Laval Institut de biologie inte&#769;grative et des syste&#768;mes ]]></institution>
<addr-line><![CDATA[Quebec ]]></addr-line>
<country>Canada</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidad Juárez del Estado de Durango Instituto de Silvicultura e Industria de la Madera ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2026</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2026</year>
</pub-date>
<numero>61</numero>
<fpage>205</fpage>
<lpage>220</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-27682026000100205&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-27682026000100205&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-27682026000100205&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Quaking aspen (Populus tremuloides) is a tree species of interest due to the potential discovery of an adaptive history in its genome, which is why the correct isolation of its DNA is essential. In this study, two extraction methods based on the NucleoSpin&#8482; Plant II kit were investigated using vegetative buds from eight paired samples. Method 1 used buffer PL1, a homogenizer, and a 30-minute incubation with RNase; Method 2 employed buffer PL2, glass beads, and a 45-minute incubation with RNase. DNA quality and quantity were assessed by spectrophotometry, gel electrophoresis, and PCR amplification. A paired t-test revealed that Method 1 yielded a significantly higher DNA concentration than Method 2 (mean difference = 71.98 ng/µL; 95% CI 17.3-126.7; p = 0.017; dz = 1.10). In contrast, no significant differences in the 260/280 ratio were observed, either by the paired t-test (mean difference = 0.10; 95% CI &#8722;0.08-0.28; p = 0.219) or by the Wilcoxon signed-rank test (median difference = +0.02; 95% CI &#8722;0.01-0.295; p = 0.25). Method 1 produced higher yields but with DNA fragmentation visible on the gel, which may interfere with some analyses. Method 2 showed a lower concentration but slightly clearer bands on the gel, indicating better DNA integrity. PCR was successful in both cases, but the higher DNA integrity in Method 2 suggests that this method is more suitable for studies requiring intact DNA. Although Method 1 yields a larger amount, Method 2 is preferable when DNA integrity is critical for genomic analysis.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El álamo temblón (Populus tremuloides) es una especie arbórea de interés debido al potencial descubrimiento de una historia adaptativa en su genoma, por lo que el aislamiento correcto de su ADN resulta esencial. En este estudio se investigaron dos métodos de extracción basados en el kit NucleoSpin&#8482; Plant II, utilizando yemas de crecimiento de ocho muestras apareadas. El método 1 empleó el tampón PL1, un homogeneizador y una incubación de 30 minutos con RNasa; el método 2 utilizó el tampón PL2, perlas de vidrio y una incubación de 45 minutos con RNasa. La calidad y cantidad del ADN se evaluaron mediante espectrofotometría, electroforesis en gel y amplificación por PCR. Una prueba t apareada reveló que el método 1 produjo una concentración de ADN significativamente mayor que el método 2 (diferencia media = 71.98 ng/µL; IC 95%: 17.3-126.7; p = 0.017; dz = 1.10). En contraste, no se observaron diferencias significativas en la relación 260/280, ya fuera mediante la prueba t apareada (diferencia media = 0.10; IC 95%: &#8722;0.08-0.28; p = 0.219) o la prueba de rangos con signo de Wilcoxon (diferencia mediana = +0.02; IC 95%: &#8722;0.01-0.295; p = 0.25). El método 1 produjo mayores rendimientos, pero con fragmentación del ADN visible en el gel, lo que puede interferir en algunos análisis. El método 2 mostró una menor concentración, pero bandas ligeramente más definidas en el gel, lo que indica mejor integridad del ADN. La PCR fue exitosa en ambos casos, aunque la mayor integridad del ADN en el método 2 sugiere que este método es más adecuado para estudios que requieren ADN intacto. Aunque el método 1 genera una mayor cantidad, el método 2 es preferible cuando la integridad del ADN es crítica para el análisis genómico.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[quaking aspen]]></kwd>
<kwd lng="en"><![CDATA[isolation]]></kwd>
<kwd lng="en"><![CDATA[PCR amplification]]></kwd>
<kwd lng="en"><![CDATA[DNA integrity]]></kwd>
<kwd lng="en"><![CDATA[genetics]]></kwd>
<kwd lng="es"><![CDATA[álamo temblón]]></kwd>
<kwd lng="es"><![CDATA[aislamiento]]></kwd>
<kwd lng="es"><![CDATA[amplificación por PCR]]></kwd>
<kwd lng="es"><![CDATA[integridad del ADN]]></kwd>
<kwd lng="es"><![CDATA[genética]]></kwd>
</kwd-group>
</article-meta>
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