The receptor preparations originate from rat brain tissue.
Autoradiography studies were carried out with [11C]KB631 on wild-type Wistar rat brain tissue and PC3/LNCaP prostate tumor slices.
In rat brain tissue, however, SCN8A protein (NaV 1.6) was easily detectable using an identical Western blot protocol (Figure 5). Figure 5 Analysis of SCN8A protein expression.
2D and 3D confocal reflectance images of micro-patterns, micro-particles, onion skins and acute rat brain tissue were obtained by this MEMS-based 3D confocal scanning microendoscope.
In addition, the bi-ligand liposomes resulted in increased expression of β-galactosidase β-gal) plasmid in rat brain tissue in comparison to the single-ligand liposomes.
We previously noted that postnatal ETS exposure, rather than prenatal exposure, resulted in reduced concentration of hindbrain DNA and increased protein/DNA ratio when rat brain tissue was studied at 9 weeks postnatal age.
The Raman spectra of three areas of Wistar rat brain tissue: the somatosensory cortex (Sc), the dorsal lateral geniculate nucleus of the thalamus (DLG) and the cerebellar cortex (Cc), excited with 785 nm and 442 nm laser line, were obtained.
We developed a multi-platform approach for the metabolome exploration of rat brain tissue, using liquid chromatography coupled with mass spectrometry (LC MS), nuclear magnetic resonance spectroscopy (NMR) and gas-chromatography coupled with mass spectrometry (GC MS).
