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Mice brain synaptosomal fractions were homogenized in 6 M guanidine-HCl containing 100 mM HEPES−NaOH (pH 7.5), 10 mM Tris (2-carboxyethyl) phosphine (TCEP), and 40 mM chloroacetamide. After heating and sonication, proteins were purified by methanol−chloroform precipitation and solubilized with 0.1% ...
ORGANISM(S): Mus Musculus (mouse) 
Brain tissues were homogenized in 6 M guanidine-HCl containing 100 mM HEPES−NaOH (pH 7.5), 10 mM Tris (2-carboxyethyl) phosphine (TCEP), and 40 mM chloroacetamide. After heating and sonication, proteins were purified by methanol−chloroform precipitation and solubilized with 0.1% 21 RapiGest SF in 50...
ORGANISM(S): Mus Musculus (mouse) 
Brain tissues were homogenized in 6 M guanidine-HCl containing 100 mM HEPES−NaOH (pH 7.5), 10 mM Tris (2-carboxyethyl) phosphine (TCEP), and 40 mM chloroacetamide. After heating and sonication, proteins were purified by methanol−chloroform precipitation and solubilized with 0.1% 21 RapiGest SF in 50...
ORGANISM(S): Mus Musculus (mouse) 
Absolute quantification of protein was performed by MALDI-LTQ using scramble internal standard (sIS) peptide. Mixtures of serial dilutions of fibrinogen peptides (final concentration: 50, 100, 250, 500 and 1000 fmol/μL), equal amounts of corresponding sIS peptides (final concentration: 500 fmol/μL) ...
ORGANISM(S): Homo Sapiens (human) 
The purpose of the study was to identify altered molecular networks in the prefrontal cortex of schizophrenia patients by comparing protein expression levels in autopsied brains of patients (n=10) and controls (n=10), using aquantitative proteomics.
ORGANISM(S): Homo Sapiens (human) 
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