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2-Dimensional Gel Electrophoresis and Mass Spectrometry.
A well accepted “gold standard” in proteomics, 2-D electrophoresis proteomics differential display analysis of protein samples followed by protein species isolation and sequencing by mass spectrometry, is offered as a service.
- Gradient strips with pH ranging from 4 to 7 are loaded via in-gel rehydration.
- First-dimension isoelectric focusing is performed at 95,000 Volt-hours.
- Second-dimension separation is done using large-format polyacrylamide slab gels with 8% to 18% thymine for 6 hours at 3 mA per gel and for 14 hours at 15 mA per gel.
- Gels are stained with SYPRO Ruby fluorescent stain.
- All gel images are scanned and compared using Z3 Image Analysis software (Compugen, Onatario, Canada).
- Protein bands of interest are excised and isolated from 2-D gels and are subjected to a 16-hour tryptic digest at 37 degrees Celsius.
- The resulting peptides are purified, desalted, and concentrated.
- The samples are analyzed by Electrospray Ionzation-Time-of-Flight Tandem Mass Spectrometry (ESI-QTOF-MS/MS) using a Micromass Quadrupole Time-of-Flight mass spectrometer equipped with a nanospray source, using either flow injection coupled to a Waters CapLC column (Waters Corp., Melford, MA) or manual acquisition using borosilicate capillaries for nanospray acquisition.
- Data is acquired over the m/z range of 400-1600 to select peptides for tandem mass spectrometry analysis. After peptides are selected, the mass spectrograph is switched to tandem mass spectrometry mode, and data is collected over the m/z range 50-2000 with variable collision energy settings.
- The data is compared against the OWL database using the MASCOT Search Engine with the species limitation and is compared against the SWISS-PROT database using ProteinLynx.
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