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Hello, I am doing disulfide bond mapping of a TNFR with a free cysteine that may be forming a covalent dimer with another protomer. After digesting the complex, I have some really large peptides...
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Akta Pure limits the number of columns per system to 5 due to the C-valve. What is the best way to add more columns to the system? I've heard of people using the loop valves to double the columns...
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