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rabbit polyclonal anti nav1 5 scn5a  (Alomone Labs)


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    Alomone Labs rabbit polyclonal anti nav1 5 scn5a
    Rabbit Polyclonal Anti Nav1 5 Scn5a, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 187 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+nav1+5+scn5a/Anti-NaV1%2E5+Antibody/10__7554_slash_elife__102027__3-343-85-90
    Average 96 stars, based on 187 article reviews
    rabbit polyclonal anti nav1 5 scn5a - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Western Blot:

    Article Title: Coordinated Tbx3/Tbx5 transcriptional control of the adult ventricular conduction system
    Article Snippet: Antibody , Rabbit polyclonal anti-CX40/GJA5 , Zymed/ Invitrogen , 36–4900 , WB (1:500). .. Antibody , Rabbit polyclonal anti-NAV1.5/SCN5A , Alomone , ASC-005 , WB (1:200). .. Antibody , Mouse monoclonal anti-KCNK3/TASK1 , Abcam , ab186352 , WB (1:1000).

    other:

    Article Title: Coordinated Tbx3/Tbx5 transcriptional control of the adult ventricular conduction system
    Article Snippet: When the hearts appeared pale and flaccid, they were removed from the Langendorff apparatus and a tip of ventricular septum below the AV annulus was microdissected out (Arnolds et al., 2012; Park and Fishman, 2011; Silverman et al., 2006) and kept in Ca2+- free Tyrode’s solution with 1 mg/ml of bovine serum albumin (Fraction XIV, Sigma Chemical Co).



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    Rabbit Polyclonal Anti Nav1 5 Scn5a, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+nav1+5+scn5a/Anti-NaV1%2E5+Antibody/10__7554_slash_elife__102027__3-343-85-90
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    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="250" height="auto" />
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    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="250" height="auto" />
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    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="250" height="auto" />
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    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="250" height="auto" />
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    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="250" height="auto" />
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    Image Search Results


    Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in <xref ref-type=Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test)." width="100%" height="100%">

    Journal: Disease Models & Mechanisms

    Article Title: Reduced connexin-43 expression, slow conduction and repolarisation dispersion in a model of hypertrophic cardiomyopathy

    doi: 10.1242/dmm.050407

    Figure Lengend Snippet: Molecular basis of electrophysiological changes in MYH7 403/+ iPSC-CMs. (A) Volcano plot of gene expression changes between MYH7 +/+ and MYH7 403/+ iPSC-CMs. FDR, false discovery rate. (B) Comparison of differentially expressed genes. Boxes show the interquartile range, whiskers show the minimum and maximum, and the median is marked with a line. N =4 differentiations. (C) Typical western blots of rhythmonome proteins for MYH7 +/+ and MYH7 403/+ . Antibody signals detected on the same membrane are grouped together. Full western blots, including replicates, are provided in Fig. S4 . (D) Summary data showing fold change in expression for rhythmonome proteins. N =3 biological replicates for all proteins, except K v 1.4, for which N =2. Bars show mean±s.e.m.; exact fold change values measured by optical densitometry (OD) are shown in C. (E) Immunohistochemistry showing expression of connexin-43 (Cx43) and α-actinin (ACTN1) in MYH7 +/+ and MYH7 403/+ cardiomyocytes. (F) Quantification of fluorescence intensity of connexin-43 and α-actinin, normalised to the number of nuclei ( n =21 images from N =3 differentiations). AU, arbitrary units. Error bars show mean±s.d. ns, not significant; * P <0.05 (unpaired two-tailed Student's t -test).

    Article Snippet: Blots were probed with the following primary antibodies: rabbit polyclonal anti-Kv1.4 (Alomone, APC-167, 1:500), rabbit polyclonal anti-Kv1.5 (Alomone, APC-004, 1:500), guinea pig polyclonal anti-Kv2.1 (Alomone, AGP-109, 1:1000), rabbit polyclonal anti-Kv4.2 (Alomone, APC-023, 1:500), guinea pig polyclonal anti-Kir2.1 (Alomone, AGP-044, 1:500), rabbit polyclonal anti-K2P3.1 (TASK1) (Alomone, APC-024, 1:500), rabbit polyclonal anti-Kir6.2 (Alomone, APC-020, 1:500), rabbit polyclonal anti-Kv11.1 (HERG) (Alomone, APC-109-F, 1:500), rabbit polyclonal anti-KCNE1 (IsK, MinK) (Alomone, APC-163, 1:500), rabbit polyclonal anti-KCNQ1 (Kv7.1) (Alomone, APC-168, 1:500), rabbit polyclonal anti-SAP97 (Thermo Fisher Scientific, PA1-741, 1:1000), rabbit polyclonal anti-Nav1.5 (Alomone, ASC-005, 1:500), rabbit polyclonal anti-Cav1.2 (Alomone, ACC-003, 1:500), rabbit polyclonal anti-connexin 43 (Cell Signalling Technology, 3512, 1:1000) and rabbit monoclonal anti-GAPDH (Cell Signalling Technology, #2118, 1:2000).

    Techniques: Gene Expression, Comparison, Western Blot, Membrane, Expressing, Immunohistochemistry, Fluorescence, Two Tailed Test, Immunofluorescence