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1 Column effluents were quantified by liquid scintillation.
2 The liquid scintillation counting (LSC) or liquid scintillation analysis (LSA) method, though widel
3 rom a reactor bioshield using combustion and liquid scintillation analysis has identified two forms o
4 s of this solution were counted in a Packard liquid scintillation analyzer; the mean radioactivity in
5 s relatively fast and can be used to produce liquid scintillation cocktails e.g., via benzene synthes
6 udied; instead of detection of activity by a liquid scintillation counter (LSC), the compounds can be
8 after specific elapsed time intervals using liquid scintillation counting (LSC) for nanomolar concen
14 isualized with X-ray film and quantitated by liquid scintillation counting after extraction from the
15 orated into the proteins, was quantitated by liquid scintillation counting after gel solubilization b
16 of radiolabeled chemical in conjunction with liquid scintillation counting and accelerator mass spect
17 210)Po in food samples using ultra low-level liquid scintillation counting and alpha-particle spectro
18 formation by mixed, undefined cultures using liquid scintillation counting and liquid chromatography
19 traction from vinegar used in preparation of liquid scintillation counting cocktails for measurements
20 radiometric approach using industry-standard liquid scintillation counting equipment that can both id
21 sing a wet chemistry digestion technique and liquid scintillation counting for (14)C activity measure
24 solids, and the supernatant was measured by liquid scintillation counting prior to injection on the
26 odium was empirically determined by HPLC and liquid scintillation counting to be 24.4 Ci/mmol, approx
27 ctrophotometrically, and cathepsin D (CD) by liquid scintillation counting using [14C] hemoglobin as
28 ures of merit similar to those obtained with liquid scintillation counting were achieved by exploitin
29 gical samples with 3H activities measured by liquid scintillation counting were utilized to develop a
31 oPak dose vial were calibrated using 4pibeta liquid scintillation counting with 3H-standard efficienc
32 he appropriate region of the gel followed by liquid scintillation counting yields an isotope ratio wh
33 ments was isolated, purified and analyzed by liquid scintillation counting, (2)H- or (13)C NMR or sel
34 d method couples solid phase extraction with liquid scintillation counting, and scintillating anion e
35 These values, measured experimentally using liquid scintillation counting, fit very well the expecte
36 he reconstituted enzyme mixture, followed by liquid scintillation counting, indicated that [14C]-8-MO
51 and activity (by [(14)C]-5-HT metabolism and liquid scintillation spectroscopy) were measured in huma
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