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Resolution: standard / high Figure 3.
A) Expression analysis of 5-HT4 receptor transcripts in embryonic and post-natal mouse tissues. RT-PCR analysis was
performed with RNA extracted from various mouse tissues (the brain (B), the eye (E),
the heart (H), and the trunk (T). The 12th, 16th, 20th GD and 1 DPN are represented in lane 1–2, 3–5, 6–8 and 9–11 respectively. The PCR
products were analysed on a 1.5% agarose gel and photographs of the ethidium bromide
stained gels are shown (upper panel). The PCR primers used for this analysis and expected
length of the PCR products are described in Materials and Methods. A positive control
was performed with β-actin primers on mRNA samples treated with reverse transcriptase.
This figure is representative of three separate determinations of mouse 5-HT4 receptor mRNA expression obtained by RT-PCR. The specificity of the PCR products were
analysed by Southern blotting using a 32P-5'-end-labeled internal primer (lower panel). A 3 h exposure of the autoradiogram
is shown. Positions of the molecular weight markers are indicated in bp. m5-HT4R, mouse 5-HT4 receptor; Marker, molecular weight marker. 3B-D) Normal receptor expression at protein
level detected using anti-5-HT4(a) and anti-5-HT4(d) antibodies in heart (B) atrium (a) myocardium (M) ventricle (V) brain, (C) in cortex
(c) hippocampus (CA1) frontal cortex (FC), during different embryonic periods and at birth. Figure 3D shows the normal expression
of 5-HT4 receptor in hippocampus of adult BALB/c mouse. Immunolabelling is shown in the left
panel and DAPI nuclear coloration in the right one.
Kamel et al. BMC Developmental Biology 2007 7:34 doi:10.1186/1471-213X-7-34 |