How do I set up my processing method to calculate the RRT of the main peak to 10kD in karat 32 software?

How do I set up my processing method to calculate the RRT of the main peak to 10kD in karat 32 software?
We’ve noticed that with some gel buffer lots, we see a dip in the baseline at 280 nm when analyzing proteins per the SDS-MW protocol. Has anyone experienced this before? We don’t always see it and are wondering what causes the dip.
As is stated in official guidance, many different types of compound and library databases can be imported into LibraryView™ software, such as Excel file (*.xls) and Third Party Library Package (*.tplp). Can somebody tell me what's the format like "tplp", which is so...
Can Resolution value be a zero?
Hi, is there a recommended standard mixture to evaluate the performance of CZE runs in a bare fused capillary with UV/Vis detector? Thanks.