<p>A and B. <i>In situ</i> hybridization shows <i>myod</i> expression in control (A) or <i>smyhc1</i>-ATG-MO (B) injected embryos at 14 hpf. Adaxial cells that give rise to slow muscles are indicated by arrows. C–F. <i>In situ</i> hybridization shows slow-specific <i>troponin C</i> expression in control (C, D) or <i>smyhc1</i>-ATG-MO (E, F) injected embryos at 24 hpf. D and F are cross sections of C and E, respectively. Arrows in D and F indicate slow muscles.</p
AbstractIt is well known that slow and fast muscles are used for long-term sustained movement and sh...
<p>Smyd1b_tv1-EGFP construct was injected into Myomesin-RFP (A, C, E) or wild type (B, D, F) zebrafi...
<p>A. Western blot analysis shows the effect of <i>smyhc1</i>-MO on the expression of the myosin hea...
<p>A–C. Anti-MyHC antibody (F59) staining shows the organization of thick filaments in trunk slow mu...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>A–C. Anti-α−actin antibody staining shows the organization of thin filaments in slow muscles of c...
<p>Anti-myomesin antibody staining shows the M-line organization in control (A), <i>smyhc1</i> knock...
<p>Zebrafish embryos co-injected with <i>smyd1a</i> E8I8 and E9I9 MOs were fixed at 28, 48 and 72 hp...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>At 48hpf, fast myosin (F310—green) and actin (phalloidin—red) staining is visible in the premyofi...
<p><b>A.</b> Smyd1b E9I9-MO was injected into Smyd1b_tv1<sup>myc</sup> or Smyd1b_tv1<sup>myc</sup> t...
<p>The <i>smyd1b</i> ATG-MO was co-injected with <i>smyd1b:zfsmyd1a<sup>myc</sup></i> or <i>smyd1b:m...
<p><b>A–C.</b> Immunostaining using sarcomeric specific antibodies against MyHC (A), α-actin (B), an...
<p>A–D. Morphological comparison of control (A, B) or BTS-treated (C, D) embryos at 48 hpf (A, C) an...
AbstractIt is well known that slow and fast muscles are used for long-term sustained movement and sh...
<p>Smyd1b_tv1-EGFP construct was injected into Myomesin-RFP (A, C, E) or wild type (B, D, F) zebrafi...
<p>A. Western blot analysis shows the effect of <i>smyhc1</i>-MO on the expression of the myosin hea...
<p>A–C. Anti-MyHC antibody (F59) staining shows the organization of thick filaments in trunk slow mu...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>A–C. Anti-α−actin antibody staining shows the organization of thin filaments in slow muscles of c...
<p>Anti-myomesin antibody staining shows the M-line organization in control (A), <i>smyhc1</i> knock...
<p>Zebrafish embryos co-injected with <i>smyd1a</i> E8I8 and E9I9 MOs were fixed at 28, 48 and 72 hp...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>Zebrafish embryos injected with <i>smyd1b</i> MO or <i>smyd1a</i> MO or both were fixed at 28, 48...
<p>At 48hpf, fast myosin (F310—green) and actin (phalloidin—red) staining is visible in the premyofi...
<p><b>A.</b> Smyd1b E9I9-MO was injected into Smyd1b_tv1<sup>myc</sup> or Smyd1b_tv1<sup>myc</sup> t...
<p>The <i>smyd1b</i> ATG-MO was co-injected with <i>smyd1b:zfsmyd1a<sup>myc</sup></i> or <i>smyd1b:m...
<p><b>A–C.</b> Immunostaining using sarcomeric specific antibodies against MyHC (A), α-actin (B), an...
<p>A–D. Morphological comparison of control (A, B) or BTS-treated (C, D) embryos at 48 hpf (A, C) an...
AbstractIt is well known that slow and fast muscles are used for long-term sustained movement and sh...
<p>Smyd1b_tv1-EGFP construct was injected into Myomesin-RFP (A, C, E) or wild type (B, D, F) zebrafi...
<p>A. Western blot analysis shows the effect of <i>smyhc1</i>-MO on the expression of the myosin hea...