The receptor preparations originate from rat brain tissue.
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).
The examples of application of multivariate DOE include using MODDE 6 software for optimization of supercritical fluid extraction, conditions for the extraction of indole alkaloids from the dried leaves of Catharanthus roseus, and GC/MS-based analysis of amino acids and organic acids in rat brain tissue samples [9, 10].
Vecka reported that fluvastatin treatment decreased the level of diphosphatidylglycerol in rat brain tissue [24].
COX coprecipitated MCT1, MCT2, and to a lesser extent, LDH from the mitochondrial fraction of rat brain tissue homogenates.
Rat brain tissue was provided by Dr. L.C. Schlichter, (TWRI, Toronto, Canada) and anti-stonin2 antibody was a gift from Dr. V. Haucke (Freie University Berlin, Germany).
It was technically impossible to obtain microvessel preparations of adequate purity from rat brain tissue at ages earlier than 9 days [18].
