<p>The gels from the top to the bottom show products from the primary, secondary, and tertiary reactions, respectively.</p
<p>Putative mutations in the pools (1, 2, 3, 4) are identified by the presence of two bands (indicat...
Lane 1: PCR Negative Control (PCR Mix). Lane 2: pAE rTES-30 Clone 1. Lane 3: pAE rTES-120 Clone 1. L...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
<p>Two representative gel pictures are shown. All bands were gel extracted and subject to sequencing...
<p>Representative agarose gels showing PCR-RFLP analysis of different single nucleotide polymorphism...
<p>PCR-RFLP agarose gel (A) after digestion with Taq1B enzyme. The 1000 bp band corresponds to the B...
<p>A: PCR products from real-time PCR experiments were analyzed on a 3% agarose gel. Lanes: 1: TaqMa...
<p>PCR amplification products of respective <i>Cryptosporidium</i> isolates were subjected to 2% aga...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>A: The PCR product amplified from the genomic DNA using the gB primers (Lane 1) and negative cont...
<p>(A): Agarose gel analysis (0.8%) of extracted gDNA by the adapted protocol. (B) : Agarose gel ana...
<p>In section a, lane 1 is the product of the first PCR step; in section b, lane 1 is the final reco...
<p>Left side of figure (column 1) represents presence or absence of novel retrogenes in 17 examined ...
Note, 150, 150°C hot-air drying; 80, 80°C hot-air drying; 40, 40°C hot-air drying; N, natural drying...
<p>(A) Control gel to ensure DNA was present. (B) Gel screening for the LSL-KrasG12D mutation at 550...
<p>Putative mutations in the pools (1, 2, 3, 4) are identified by the presence of two bands (indicat...
Lane 1: PCR Negative Control (PCR Mix). Lane 2: pAE rTES-30 Clone 1. Lane 3: pAE rTES-120 Clone 1. L...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
<p>Two representative gel pictures are shown. All bands were gel extracted and subject to sequencing...
<p>Representative agarose gels showing PCR-RFLP analysis of different single nucleotide polymorphism...
<p>PCR-RFLP agarose gel (A) after digestion with Taq1B enzyme. The 1000 bp band corresponds to the B...
<p>A: PCR products from real-time PCR experiments were analyzed on a 3% agarose gel. Lanes: 1: TaqMa...
<p>PCR amplification products of respective <i>Cryptosporidium</i> isolates were subjected to 2% aga...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>A: The PCR product amplified from the genomic DNA using the gB primers (Lane 1) and negative cont...
<p>(A): Agarose gel analysis (0.8%) of extracted gDNA by the adapted protocol. (B) : Agarose gel ana...
<p>In section a, lane 1 is the product of the first PCR step; in section b, lane 1 is the final reco...
<p>Left side of figure (column 1) represents presence or absence of novel retrogenes in 17 examined ...
Note, 150, 150°C hot-air drying; 80, 80°C hot-air drying; 40, 40°C hot-air drying; N, natural drying...
<p>(A) Control gel to ensure DNA was present. (B) Gel screening for the LSL-KrasG12D mutation at 550...
<p>Putative mutations in the pools (1, 2, 3, 4) are identified by the presence of two bands (indicat...
Lane 1: PCR Negative Control (PCR Mix). Lane 2: pAE rTES-30 Clone 1. Lane 3: pAE rTES-120 Clone 1. L...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
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