<p>(A) Restriction enzyme map of <i>PstI</i> and <i>TaqI</i>. <i>PstI</i> and <i>TaqI</i> sites are located approximately 0.7 kb and 2.5 kb up-stream of the transgene, respectively. The bold lines indicate location of the 0.7 kb probe. Primers (OUT1 and IN1) were used for the 2nd IPCR. (B) Southern blot analysis. In addition to the expected size, an additional band (indicated by arrows) was detected by <i>PstI</i> (1.4 kb) and <i>TaqI</i> (3.5 kb) digestion. (C) <i>PstI</i> digested DNA fragment (1.4 kb) was eluted from the gel, purified and IPCR was carried out. The expected size (1 kb) of the 2nd PCR product was obtained.</p
<p>Specific restriction sites were used to distinguish between embryonic OCT4A transcript and differ...
<p>(A) Expected <i>GFP</i>-hybridizing gDNA restriction fragment sizes for HR reporter at the <i>ROS...
<p>(A) <i>Cdh22</i> locus. The first transposon insertion was screened using the primer pair 1B5′/1B...
<p>(A) Sequence of the PCR product. PstI and BamHI restriction sites are shown in boxes. Restriction...
<p>The diagram illustrates the IPCR strategy used to obtain sequences flanking the T-DNA insertion s...
<p>Cloning of a 590 bp foreign DNA was performed using SacI and HindIII restriction sites located wi...
<p>Southern hybridization of genomic DNA (gDNA) of <i>S. ratti</i> from stably transformed lines pro...
a<p>Bold, underlined, and italic letters <i>Xba</i>I, <i>Hind</i>III, and <i>Pst</i>I restriction si...
<p>(<b>A</b>) Digestion of the uGCR chrV divides the uGCR chrV into left telomeric, internal, and ri...
<p>500 ng DNA were digested with different restriction enzymes for 2 h at 37°C and electrophoresed. ...
<p>Arrows indicate the positions of the PCR DsRed primers. XbaI and DraI were restriction enzyme dig...
<p>Sites for restriction enzymes BamHI (GGATCC), XhoI (CTCGAG), XbaI (TCTAGA) and EcoRV (GATATC) are...
<p>Tail DNA for the transgenic lines indicated above the lanes were amplified for the gene segment i...
<p>(A) Schematic map of plasmid pHS300. The deleted region, found in plasmid DNA isolated from vacci...
<p>A, generation of sticky-end fragments and cloning into pWXY1.0 by IRDL cloning. The <i>JcDGAT2</i...
<p>Specific restriction sites were used to distinguish between embryonic OCT4A transcript and differ...
<p>(A) Expected <i>GFP</i>-hybridizing gDNA restriction fragment sizes for HR reporter at the <i>ROS...
<p>(A) <i>Cdh22</i> locus. The first transposon insertion was screened using the primer pair 1B5′/1B...
<p>(A) Sequence of the PCR product. PstI and BamHI restriction sites are shown in boxes. Restriction...
<p>The diagram illustrates the IPCR strategy used to obtain sequences flanking the T-DNA insertion s...
<p>Cloning of a 590 bp foreign DNA was performed using SacI and HindIII restriction sites located wi...
<p>Southern hybridization of genomic DNA (gDNA) of <i>S. ratti</i> from stably transformed lines pro...
a<p>Bold, underlined, and italic letters <i>Xba</i>I, <i>Hind</i>III, and <i>Pst</i>I restriction si...
<p>(<b>A</b>) Digestion of the uGCR chrV divides the uGCR chrV into left telomeric, internal, and ri...
<p>500 ng DNA were digested with different restriction enzymes for 2 h at 37°C and electrophoresed. ...
<p>Arrows indicate the positions of the PCR DsRed primers. XbaI and DraI were restriction enzyme dig...
<p>Sites for restriction enzymes BamHI (GGATCC), XhoI (CTCGAG), XbaI (TCTAGA) and EcoRV (GATATC) are...
<p>Tail DNA for the transgenic lines indicated above the lanes were amplified for the gene segment i...
<p>(A) Schematic map of plasmid pHS300. The deleted region, found in plasmid DNA isolated from vacci...
<p>A, generation of sticky-end fragments and cloning into pWXY1.0 by IRDL cloning. The <i>JcDGAT2</i...
<p>Specific restriction sites were used to distinguish between embryonic OCT4A transcript and differ...
<p>(A) Expected <i>GFP</i>-hybridizing gDNA restriction fragment sizes for HR reporter at the <i>ROS...
<p>(A) <i>Cdh22</i> locus. The first transposon insertion was screened using the primer pair 1B5′/1B...