tsbatth.bsky.social
Co-founder/CEO KPL ApS , #Proteomics researcher in Copenhagen, Denmark at Københavns Universitet, NNF Center for Protein Research #science, #technology, #culture, memes and vibes.
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Is that to avoid saying it's unpaid? 😂🤦🏽♂️
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No details on compensation?
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Best of luck Bini, your proteomic posts, insights and discussions are always valuable so I hope we get to keep seeing more of that.
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In the meantime, if anybody needs any assistance currently with their mass spec proteomics project design, method review, data analysis, or result interpretation, please feel free to reach out.. It would be my pleasure to be of assistance.. I am also available for consulting/freelancing.. 5/6
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Wouldn't the three internal arginines and a histidine provide sufficient charges to the peptide for fragmentation? Maybe the charge state of this spectrum is too low??
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Is it still possible to get the output reports similar to the older versions with # unique proteins, peptides, intensities, MS1/2 signal ratios, peak widths etc..? The new reports are cool as well, but practically the info in the old reports were really useful. Congrats again on the new version!!
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Congrats! Very cool results and very useful! Do you think there is a way to do the opposite, ie. increase O-acylation while reducing N-acylation ?
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I've tried 3 different software now. I gave them a "positive control" where we know the protein "docks" with one molecule and a "negative control" of a molecule that does not. The software can't help themselves and keep predicting the negative control with better affinity!
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If you want to know more, have a look at the paper – or read the great News&Views article by @christatesterink.bsky.social www.nature.com/articles/d41...