Protocol Step: Marelli_protocol Sample Prep

demo
Name Marelli_protocol Sample Prep
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Description An organellar 20KgP fraction was subjected to isopycnic density gradient centrifugation and analyzed by SDS-PAGE and Coomassie blue staining. Fractions enriched for peroxisomes (EP) or mitochondria (M) were identified by Western blotting. Equal amounts of protein derived from each of the hypotonically lysed M and EP fractions were combined and analyzed by ICAT MS/MS.
Max input data per instance 0
Max input material per instance 1
Output data per instance 0
Output material per instance 1
ApplicationLSIDTemplate ${RunLSIDBase}:SamplePreparation.Default
OutputMaterialNameTemplate ${InputName}.Modified
ApplicationNameTemplate SamplePreparation
OutputMaterialLSIDTemplate ${RunLSIDBase}:${InputName}.Modified
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Protocol Predecessors
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Description
Marelli_protocol (LCMS2)1Prepare and run LCMS, producing one mzXml file per input sample.
Protocol Successors
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Description
Marelli_protocol LC MS230ICAT-labeled peptides were analyzed by µLC-ESI-MS/MS. Peptides were separated by on-line reversed-phase chromatography using a 75 µm x 10 cm self-packed Magic C18AQ column (Michrom BioResources) at a flow rate of 300 nL/min. Peptide fragmentation by collision-induced dissociation was performed in an automated fashion using the dynamic-exclusion option from the full-range MS spectra or by GPFm/z using an ion trap mass spectrometer (Thermofinnigan; Yi et al., 2002).