<p>Lane 1–9: PCR amplified <i>Glut1</i> and <i>α-actin</i> fragments in pleopod, gill, stomach, midgut, heart, lymphoid organ, nervous tissue, hepatopancreas, and hemolymph. C: PCR reaction control which is set up in the same way as the experimental PCRs, but without template DNA added.</p
<p>Expression is shown for the genes (A) IL-1β, (B) IL-8, (C) TGF-β, (D) TLR-3, (E) TLR-9 and (F) TL...
<p><i>poP2RX7</i> mRNA expression in healthy <i>P. olivaceus</i> tissues was analyzed by qRT-PCR wit...
<p>A) P. <i>dolloi</i> gut cryosection stained with the nuclear stain DAPI (blue) showing the charac...
<p>A plasmid DNA of CREB partial cDNA was used as positive control (PC) and PCR reaction without RT ...
<p>Total RNA extracted from the head plus thoracic segments (head+thorax) and abdominal tissues were...
<p>Primers used for the top panel amplify only ap-GnRHR-L; primers used for the second panel amplify...
<p>The <i>T</i>. <i>tridentatus GAPDH</i> transcript was used as internal standard. I, intestine; L:...
<p>(A) Analysis of <i>Es-DWD1</i> gene expression relative to <i>β-actin</i> in different Chinese mi...
<p>(A) Results of the <i>β-actin</i> and <i>lipL32</i> targeted duplex amplification assay when test...
<p>The samples represent goat heart, liver, spleen, kidney, brain, <i>longissimus dorsi</i> muscle, ...
<p>Western blotting analysis and quantification of GLUT1 protein levels in HT-1376 and UM-UC-3 cells...
<p>The amplification of β-actin was used as an internal control. Gene names are indicated on the lef...
Lanes 2 and 3 are RT-PCR products amplified from liver (L) and intestine (I) cDNAs for the gene; lan...
We report a rapid technique, based on the polymerase chain reaction (PCR), for the direct targeting,...
<p>1. Eye 2. Tongue 3. Operculum 4. Dorsal fin 5. Dorsal skin 6. Caudal skin 7. Caudal fin 8. Ventra...
<p>Expression is shown for the genes (A) IL-1β, (B) IL-8, (C) TGF-β, (D) TLR-3, (E) TLR-9 and (F) TL...
<p><i>poP2RX7</i> mRNA expression in healthy <i>P. olivaceus</i> tissues was analyzed by qRT-PCR wit...
<p>A) P. <i>dolloi</i> gut cryosection stained with the nuclear stain DAPI (blue) showing the charac...
<p>A plasmid DNA of CREB partial cDNA was used as positive control (PC) and PCR reaction without RT ...
<p>Total RNA extracted from the head plus thoracic segments (head+thorax) and abdominal tissues were...
<p>Primers used for the top panel amplify only ap-GnRHR-L; primers used for the second panel amplify...
<p>The <i>T</i>. <i>tridentatus GAPDH</i> transcript was used as internal standard. I, intestine; L:...
<p>(A) Analysis of <i>Es-DWD1</i> gene expression relative to <i>β-actin</i> in different Chinese mi...
<p>(A) Results of the <i>β-actin</i> and <i>lipL32</i> targeted duplex amplification assay when test...
<p>The samples represent goat heart, liver, spleen, kidney, brain, <i>longissimus dorsi</i> muscle, ...
<p>Western blotting analysis and quantification of GLUT1 protein levels in HT-1376 and UM-UC-3 cells...
<p>The amplification of β-actin was used as an internal control. Gene names are indicated on the lef...
Lanes 2 and 3 are RT-PCR products amplified from liver (L) and intestine (I) cDNAs for the gene; lan...
We report a rapid technique, based on the polymerase chain reaction (PCR), for the direct targeting,...
<p>1. Eye 2. Tongue 3. Operculum 4. Dorsal fin 5. Dorsal skin 6. Caudal skin 7. Caudal fin 8. Ventra...
<p>Expression is shown for the genes (A) IL-1β, (B) IL-8, (C) TGF-β, (D) TLR-3, (E) TLR-9 and (F) TL...
<p><i>poP2RX7</i> mRNA expression in healthy <i>P. olivaceus</i> tissues was analyzed by qRT-PCR wit...
<p>A) P. <i>dolloi</i> gut cryosection stained with the nuclear stain DAPI (blue) showing the charac...
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