The validation of aerated weighted cohesion (WSA) as a flowability indicator was authenticated by comparing the conducted parameter with established measured Hausner ratio (HR) and angle of repose (AoR).
High-resolution (HR) high-angle annular dark field scanning TEM (HAADF-STEM) measurements also confirm the successful sequential cation exchange from parent CdSe/CdS dot core/rod shell NRs into product CISe/CIS dot core/rod shell NRs via intermediate Cu2Se/Cu2S dot core/rod shell NRs.
The sheared large DNA fragments were end-repaired with a DNA terminator kit (Lucigen) for 30 min at room temperature followed by heat inactivation at 70°C for 15 min. The end-repaired large fragment DNA was fractionated on a CHEF-Mapper system (BioRad) in 1% PFGE agarose, 0.5X TBE, using the following conditions: 6 V/cm, 0.1 - 2 s time ramp, 11 hrs, 120° angle, and 14°C.
High resolution magic angle spinning (HR MAS) MRS of ex vivo tissue samples has been particularly useful, as it allows assessment of individual choline metabolites in intact tissue specimens.
High-resolution H MRS analyses were performed on intact EOC xenograft specimens using a high-resolution Magic Angle Spinning (HR MAS) technique on a Bruker Avance spectrometer at 9.4 T (Karlsruhe, Germany) as described in our previous study (Canese et al, 2012).
High-resolution scanning electron microscopy (HR-SEM), glancing incidence angle X-ray powder diffraction (GIXRD) and small-angle X-ray scattering (SAXS) techniques were employed to characterise the surface structure and morphology of catalyst materials.
In the current paper, 1H High Resolution Magic Angle Spinning (HR-MAS) NMR spectroscopy was directly applied to G. lamblia trophozoite suspensions to analyze the detectable small metabolites with a minimum of intervention.
700 MHz 1D high-resolution magic angle spinning (HR-MAS) proton NMR spectra of intact liver tissue from four months old wild-type mice (n = 6), mutant 569 mice (n = 3), mutant 391 mice (n = 6), and wild-type mice fed on a high-fat diet (n = 3) were measured.
One part was examined using high-resolution magic angle spinning (HR-MAS) MR spectroscopy while another part was analyzed using gene expression microarrays.
High-resolution magic angle spinning (HR-MAS) magnetic resonance (MR) spectroscopy of tissue biopsies provides detailed information on their metabolic composition [ 2].
High-resolution magic angle spinning (HR-MAS) MRS has proven to be a useful technique for assessment of choline (Cho) metabolism, as it allows detection of individual Cho metabolites in intact tissue specimens.
