ok so do you trust an area percent from a shallow gradient
#hplc-massspec 2025-10-09
how would a truncation sequence show up
run a blank
the first peak is the solvent. it is always the solvent
coming back after 16 months, what changed in how you read these
plus 0.98 is deamidation
quick one is uv at 214 or 280 better for peptides
ask for the trace
how do you tell co-elution from a clean single peak
update on the earlier thing baseline is drifting badly, is that the column or the mobile phase
is there any point running a blank if the sample is the question
if somebody says they ran a mass spec and does not show you a spectrum, that is a claim, not a result
a warm transit can put a visible degradant peak on a chromatogram. that is what 19 days at ambient does
integration choices move the number by a few tenths easily. that is most of your inter-lab variance