<p>A. Heart RNA from biological replicates (DS mice, n = 4; WT mice, n = 5) were used to generate two independent cDNAs per animal. The cDNAs were assayed using qPCR in quadruplicate with two independent <i>Scn5a</i> TaqMan primer sets and normalized to 18s RNA. B. Western blots of membrane proteins isolated from DS and WT ventricular CMs. 50 µg of protein was loaded in each lane, and probed with anti-Na<sub>v</sub>1.5 (Mohler 1:1000), and anti-α-actin (Sigma 1:500), which served as the loading control. C. Quantification of Na<sub>v</sub>1.5 expression normalized to α-actin expression.</p
<p><b>(A)</b> Assessment of ventricular mRNA expression by quantitative real-time PCR of atrial natr...
Cardiac sodium channels are responsible for conduction in the normal and diseased heart. We aimed to...
The cardiac voltage-gated sodium channel, Nav1.5, plays a central role in cardiac excitability and i...
<p><b>A.</b> Representative Western blots showing the expression levels of Na<sub>v</sub>1.5 in WT m...
(A) mRNA levels of Scn5a (Nav1.5) sodium channel, Slc8a1 (Ncx1) sodium calcium exchanger, Pln, Cacna...
<p><b>A</b>. Detection of ~240 kDa bands corresponding to Ca<sub>V</sub>1.2 in ventricular tissue fr...
(A) Western blot with anti-Nav1.5 and anti-NCX1 protein expression in the heavy SR fractions from 5 ...
D ow nloaded from Aim: The aim of this study was to analyze the mRNA expression levels and protein d...
<p>(A) Protein lysates from four different WT and MHC-CnA ventricles were analyzed for Na<sub>V</sub...
<p>(A) Atrial; (B) ventricular. Connexins and sodium channels genes expression levels were assessed ...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
Background: Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associa...
<p>Gene expression was normalized using <i>cyclophilin A</i> and <i>Rplp1</i>. MCT, monocarboxylate ...
BACKGROUND: Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associa...
<p><b>A.</b> Representative I<sub>Na</sub> traces (protocol in <i>inset</i>) obtained from ventricul...
<p><b>(A)</b> Assessment of ventricular mRNA expression by quantitative real-time PCR of atrial natr...
Cardiac sodium channels are responsible for conduction in the normal and diseased heart. We aimed to...
The cardiac voltage-gated sodium channel, Nav1.5, plays a central role in cardiac excitability and i...
<p><b>A.</b> Representative Western blots showing the expression levels of Na<sub>v</sub>1.5 in WT m...
(A) mRNA levels of Scn5a (Nav1.5) sodium channel, Slc8a1 (Ncx1) sodium calcium exchanger, Pln, Cacna...
<p><b>A</b>. Detection of ~240 kDa bands corresponding to Ca<sub>V</sub>1.2 in ventricular tissue fr...
(A) Western blot with anti-Nav1.5 and anti-NCX1 protein expression in the heavy SR fractions from 5 ...
D ow nloaded from Aim: The aim of this study was to analyze the mRNA expression levels and protein d...
<p>(A) Protein lysates from four different WT and MHC-CnA ventricles were analyzed for Na<sub>V</sub...
<p>(A) Atrial; (B) ventricular. Connexins and sodium channels genes expression levels were assessed ...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
Background: Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associa...
<p>Gene expression was normalized using <i>cyclophilin A</i> and <i>Rplp1</i>. MCT, monocarboxylate ...
BACKGROUND: Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associa...
<p><b>A.</b> Representative I<sub>Na</sub> traces (protocol in <i>inset</i>) obtained from ventricul...
<p><b>(A)</b> Assessment of ventricular mRNA expression by quantitative real-time PCR of atrial natr...
Cardiac sodium channels are responsible for conduction in the normal and diseased heart. We aimed to...
The cardiac voltage-gated sodium channel, Nav1.5, plays a central role in cardiac excitability and i...