<p>Uncut PCR product from <i>L. tropica</i> MHOM/PS/18JnMF4 ( = LRC-L891) was used as a control and molecular sizes were compared with a 50 bp molecular weight ladder (MW), nd = not done; c) of the PCR products from the Phosphoglucomutase (PGM) genes of the leishmanial reference strain <i>L. tropica</i> LRC-L863 and local Palestinian strains after single digestion with the endonuclease <i>MboI</i>. Only the heavier differentiating band is shown. Uncut PCR product from <i>L. tropica</i> MHOM/PS/02/79JnF20 ( = LRC-L885) was used as a control and molecular sizes were compared with a 50 bp molecular weight ladder (MW).</p
<p>Silver-stained 5% polyacrylamide gels showing: <b>A</b>) ITS1-PCR: Lane M—Promega standard molecu...
<p>(A) PCR products of first amplification of HSP 70 (234) targeting analyzed by electrophoresis pol...
<p>1: molecular-weight marker (50-bp DNA ladder); 2. empty; 3–8. mixture of human DNA and 100 (3), 5...
<p>Lanes 1–8 were 10-fold dilutions of leishmanial genomic DNA from 10 ng to 1 fg per reaction. Lane...
Figure S1. Agarose gel electrophoresis of PCR products. Reactions were performed using TopTaq Master...
<p>PCR products were separated by electrophoresis in 2% agarose gels and stained with ethidium bromi...
Multilocus enzyme electrophoresis is the gold standard for identification of Leishmania species and ...
<p>Agarose gel electrophoresis showing PCR products using the LeF/LeR primers for <i>Leishmania</i> ...
<p>(A) PCR amplification products of the <i>Leishmania</i> kDNA minicircle conserved region from cut...
<p>Top panel 300 bp, <i>Leishmania</i> ITS1 PCR product. Bottom panel shows the HAE<i>III</i> restri...
<p>Nested PCR amplification products from serial dilution curves of DNA from <i>L</i>. <i>V</i>. <i>...
Multi-locus enzyme electrophoresis is the current gold standard for the genetic characterisation of ...
In this study, two-dimensional gel electrophoresis (2-DE) method was applied to determine and compar...
Many laboratory methods are used to diagnose leishmaniasis because it is characterized by varied sym...
In this study, PCR assays targeting different Leishmania heat-shock protein 70 gene (hsp70) regions,...
<p>Silver-stained 5% polyacrylamide gels showing: <b>A</b>) ITS1-PCR: Lane M—Promega standard molecu...
<p>(A) PCR products of first amplification of HSP 70 (234) targeting analyzed by electrophoresis pol...
<p>1: molecular-weight marker (50-bp DNA ladder); 2. empty; 3–8. mixture of human DNA and 100 (3), 5...
<p>Lanes 1–8 were 10-fold dilutions of leishmanial genomic DNA from 10 ng to 1 fg per reaction. Lane...
Figure S1. Agarose gel electrophoresis of PCR products. Reactions were performed using TopTaq Master...
<p>PCR products were separated by electrophoresis in 2% agarose gels and stained with ethidium bromi...
Multilocus enzyme electrophoresis is the gold standard for identification of Leishmania species and ...
<p>Agarose gel electrophoresis showing PCR products using the LeF/LeR primers for <i>Leishmania</i> ...
<p>(A) PCR amplification products of the <i>Leishmania</i> kDNA minicircle conserved region from cut...
<p>Top panel 300 bp, <i>Leishmania</i> ITS1 PCR product. Bottom panel shows the HAE<i>III</i> restri...
<p>Nested PCR amplification products from serial dilution curves of DNA from <i>L</i>. <i>V</i>. <i>...
Multi-locus enzyme electrophoresis is the current gold standard for the genetic characterisation of ...
In this study, two-dimensional gel electrophoresis (2-DE) method was applied to determine and compar...
Many laboratory methods are used to diagnose leishmaniasis because it is characterized by varied sym...
In this study, PCR assays targeting different Leishmania heat-shock protein 70 gene (hsp70) regions,...
<p>Silver-stained 5% polyacrylamide gels showing: <b>A</b>) ITS1-PCR: Lane M—Promega standard molecu...
<p>(A) PCR products of first amplification of HSP 70 (234) targeting analyzed by electrophoresis pol...
<p>1: molecular-weight marker (50-bp DNA ladder); 2. empty; 3–8. mixture of human DNA and 100 (3), 5...