Along with everyone else, the mass spectrometry facility is feeling the effect of inflation and prices rises. For the first time since 2018 we have had to increase our mass spectrometry access charges. These are below, and also on the services page of our website
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The Biomolecular Sciences Building is back up and running after the devastating fire 3 years ago. Reception has now moved from its temporary home in the Willie Russell Laboratories back in to the BMS Building. All samples and correspondance should be sent to: BSCR Mass Spectrometry and Proteomics Facility, Biomolecular Sciences Building, University of St…
Our workhorse 4800 has given up after many years faithful service. Unfortunately there is just not the demand for MALDI proteomics to justify the costs in fixing it, so we will no longer be able to offer MALDI analysis as a service.
Our new mass spectrometer is installed and operational. With BBSRC 19Alert equipment grant funding we purchased a Thermoscientific Fusion Lumos orbitrap mass spectrometer with a standard HPLC (Vanquish) and nano LC (Ultimate). We look forward to familiarising ourselves with the instrument and getting some nice analysis on it soon
We have recently upgraded our mascot server hardware. The new link to the server is https://newbsrcmascot.st-andrews.ac.uk/mascot/ . The login and password will remain the same as before.
The BSRC mass spectrometry and proteomics facility is fully open and able to analyse your samples. We aim to have at least one member of staff in the facility each day, and can always be contacted on massspec @ st-andrews.ac.uk
We have had a few issues with the on-line sample submission that we set up at the start of the year. Whilst we sort out these problems we have reverted back to your previous paper submission. Links to the form to print out can be found in the sample submission page.
S-Trap™ : An easy-to-use spin column method for sample processing(S-Trap-method). Application includes: sample concentration, clean up and digestion with reduced variability. Use S-Trap™ micros for sub-microgram to 50 µg scales. S-Trap™ minis for 50 – 300 µg and S-Trap™ midis for larger scales (300 µg to multiple mg).
In-solution digestion method is usually a method of choice for comparative proteomic studies. Compared to in-solution digestion, in-gel digestion can be more complicated as it usually involves dicing of gel slices, extensive washing/destaining, and peptide extraction after digestion. These multiple steps may increase the variability and render in-gel digestion less reproducible than in-solution digestion. In…
Excised gel bands are cut into small pieces and processed for In gel digestion. In comparative proteomic studies, it is important to know the variability associated with sample preparation. Sample preparation steps differs based on the complexity and chemistry of the sample. In this website we provide few protocols, however please discuss with our staff…