I'm having difficulties to make sense probes for whole mount in situ
hybridization. There are no big differences in staining patterns
between my sense and antisense probes. Is anyone familiar with the
problem? What can I do to prevent this?
Research Group Neural Circuit Development and Regeneration
Department of Biology, Katholieke Universiteit Leuven (K.U.Leuven)
Naamsestraat 61, bus 2464
B-3000 Leuven, Belgium