Additionally, most often detection is carried out
on lysed cell samples, so a significant amount of information is lost.
Not exact matches
Cells were
lysed on ice using lysis buffer (10 mM Tris - HCl pH 7.4, 150 mM NaCl, 1 % Triton X-100, protease inhibitor mix G (Serva) and 2 mM Na3VO4).
Cultured cells were
lysed in radioimmunoprecipitation assay (RIPA) buffer (50 μl RIPA per 1 × 106 cells; 50 mM Tris / HCl; 150 mM NaCl, 1 % Triton X-100, 1 mM EDTA, 1 mM NaF, 1 mM Na3VO4, 1 μg / ml leupeptin and 1 μg / ml pepstatin) for 1 h
on ice, and insoluble debris was removed by centrifugation.
Cells were washed with ice - cold PBS,
lysed for 15 minutes
on ice with M - PER protein extraction reagent (Pierce), scraped, and spun at 14,000 rpm for 10 minutes at 4 °C.
Supplies Serratia peptidase enzyme to help protect sensitive GI tissues from irritation and lysozyme for its unique
lysing action
on bacterial and yeast cell walls
A view from the streets and the chancelleries:
Lyse Doucet attempts a perspective
on the conflict of our century