Phenom Support Answers

A collection of questions that received good ratings and feedback from our customers.

• Are securityLink fittings Biocompatible?
• Are the guard columns for bioZen also biocompatible?
• Are the ionic capacities of Strata XL ion-exchange sorbents different from Strata X ion-exchange sorbents due to their difference in surface area?
• At what pressure are Verex 20mm Pressure release seals designed to break?
• Can a contaminated gas supply possibly cause GC columns to have higher bleed?
• Can Aeris be scaled-up for preparative applications?
• Can alternative lysis and/or load buffers be used in the Clarity OTX extraction protocol?
• Can EZ:faast analyze carnitine?
• Can EZ:faast be used to analyze organic acids such as citrate and succinate?
• Can EZ:faast be used to analyze phosphoamino acids?
• Can EZ:faast for the analysis of amino sugars?
• Can I apply a second elution on Phree to improve analyte recovery?
• Can I elute phospholipids from Phree?”
• Can I prepare my own Low Molecular Weight Protein Standards?
• Can I purchase the EZ:faast kit reagents separately?
• Can I redissolve proteins after protein precipitation by Impact?
• Can I reuse my SPE (Strata or Strata-X) tubes?
• Can I reverse flush my Yarra column?
• Can I reverse flush the SEC column?
• Can I reverse or back flush my Kinetex column?
• Can I run a gradient in normal phase?
• Can I switch from non-denaturing to denaturing conditions in SEC and back again?
• Can I use 2 columns in series to increase the molecular weight range of my analysis in GFC?
• Can I use a capillary column with a packed column inlet?
• Can I use a partial plate of Impact?
• Can I use a salt buffer as an elution to an ion exchange method?
• Can I use acetone or DCM on silica based column like Luna or Kinetex?
• Can I use an acid other than formic acid in the Phree protocol?
• Can I use methanol in my HILIC method as the organic solvent?
• Can I use packed columns for GC/MS analysis?