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Proto-myofibroblasts were treated with siRNA, washed with ice-cold HEPES-saline (20 mM HEPES-NaOH [pH 7.5], 137 mM NaCl), detached by Accutase (Nacalai Tesque), and lysed in guanidine-TCEP buffer (8 M guanidine-HCl, 100 mM HEPES-NaOH [pH 7.5], 10 mM TCEP, 40 mM CCA). After heating and sonication, 20...
ORGANISM(S): Mus Musculus (mouse) 
Proto-myofibroblasts were treated with siRNA, washed with ice-cold HEPES-saline (20 mM HEPES-NaOH [pH 7.5], 137 mM NaCl), detached by Accutase (Nacalai Tesque), and lysed in guanidine-TCEP buffer (8 M guanidine-HCl, 100 mM HEPES-NaOH [pH 7.5], 10 mM TCEP, 40 mM CCA). After heating and sonication, 20...
ORGANISM(S): Mus Musculus (mouse) 
Cardiac myofibroblasts retrovirally transduced with FLAG-VGLL3 or control vector were fixed with 0.1% PFA and lysed in a HEPES-RIPA buffer (20 mM HEPES-NaOH [pH 7.5]/1 mM EGTA/1 mM MgCl2/150 mM NaCl/0.25% sodium deoxycholate/0.05% SDS/1% NP-40) containing protease inhibitors (1:100), phosphatase inh...
ORGANISM(S): Mus Musculus (mouse) 
For immunoprecipitation to detect the endogenous interaction between VGLL3 and DDX5, cardiac myofibroblasts were fixed with 0.1% PFA and lysed in IP buffer [20 mM HEPES­NaOH (pH 7.5)/1 mM EGTA/1 mM MgCl2/150 mM NaCl /5% glycerol/1% NP­40] containing protease inhibitors (1:100) and phosphatase inhibi...
ORGANISM(S): Mus Musculus (mouse) 
For immunoprecipitation to detect the endogenous interaction between VGLL3 and EWSR1, cardiac myofibroblasts were fixed with 0.1% PFA and lysed in IP buffer [20 mM HEPES­NaOH (pH 7.5)/1 mM EGTA/1 mM MgCl2/150 mM NaCl /5% glycerol/1% NP­40] containing protease inhibitors (1:100) and phosphatase inhib...
ORGANISM(S): Mus Musculus (mouse) 
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