<p>(A) Total RNAs were extracted from <i>Oregon</i> R, <i>Axn<sup>EY10228</sup></i>, <i>slmb<sup>00295</sup></i>, and <i>nkd<sup>2</sup></i> 2<sup>nd</sup> instar larvae. The mRNA levels of <i>Met</i>, <i>gce</i> and <i>Kr-h1</i> were assessed by quantitative real-time PCR and normalized to <i>rp49</i> mRNA. Values shown are the means of 4 independent experiments ± standard deviations. (B) The same total RNAs described in [A] were used as the templates for a 30-cycle reverse transcriptional PCR. The RT-PCR products were analyzed by DNA agarose gel electrophoresis.</p
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