Phenom Support Answers
A collection of questions that received good ratings and feedback from our customers.
- How much sorbent is packed inside 00M-S033-B0-CB Strata-X 25um On-Line Cartridge 20 x 2.0mm?
- How sensitive is the EZ:faast method to pH?
- How should a column be cleaned if it is typically used to analyze protein samples?
- How should I choose the Claricep flash column series based on the instruments?
- How should I couple my GPC columns in series?
- How should I keep the linear velocity the same when I change the dimension of my column?
- How should I optimize my method on an Aeris column?
- How should I select an inlet liner for my GC analysis?
- How should I select the appropriate dSPE sorbents from those available within the RoQ QuEChERs product range?
- How should I select which ferrule material is best for my application?
- How should I select which ionic form of Rezex is most suitable for my application?
- How should I store my Chirex 3126 column?
- How should I store my HPLC columns?
- How should the amino acid standards in the EZ:faast kit be stored?
- How specific is Phree for removing only phospholipids?
- How to find the number of possible enantiomer for a given molecule?
- How will protein binding affect my SPE?
- How will the sample diluent affect HILIC separations?
- How would you prepare your buffers for IEX methods.
- How would you recommend storing a column which has been used in SFC mode?
- I am about to start working on a new HPLC method, is there anything you would recommend I do with my system prior to starting work?
- I am analysing OPA/FMaration initially looks good, but after 50 injections my peaks are broadening and I am loosing resolution. What could be the problem?
- I am considering using an ion-pairing mechanism with a non-C18 reversed phase column, is it possible?
- I am currently developing a new method in normal phase and I am experiencing problems with reproducibility, what can I do?
- I am currently developing a new method in normal phase and I am having problems getting retention, what should I consider?
- I am currently working on epoxides, do you have any advice for working with reactive polymers?
- I am not regulated by either the AOAC or EN standards. Which extraction kit should I choose?
- I am not seeing the efficiency increase I expected from switching to Kinetex, what could be the problem?
- I am observing a steady, low backpressure in my LC method what could be causing this?
- I am planning to use a 1 mm ID column, what product do you recommend to protect it?