Certified Pre-Owned Triple Quadrupole LC / MS System Ultivo
Certified Pre-Owned Ultivo Triple Quadrupole LC / MS - Includes G6465B analytical HW, PC, install, intro 1Y SW upgrade/phone assist
Product Specifications
Description
Ultivo is a compact, stackable triple quadrupole LC/MS/MS that eliminates the MS footprint by incorporating the mass spectrometer into the HPLC stack
Representing a transformative approach to triple quadrupole mass spectrometry, Ultivo provides the fit-for-purpose, straightforward, and rugged LC/MS analysis you expect from larger comparable systems, but at a fraction of their size
Multiple ion source configurations available, including Agilent Jet Stream and traditional ESI
VacShield eliminates the need to vent the system while performing ion injector maintenance, minimizing maintenance downtime and increasing laboratory efficiency
Cyclone ion guide compresses the ion beam without loss of signal, resulting in higher ion transmission efficiencies and enhanced data quality
Vortex collision cell provides efficient dissociation of ions in the cell, improved focusing and transmission of ions, and rapid clearance of the cell between mass transitions, thereby allowing for more MRMs/sec, zero crosstalk, and greater confidence in results by removing noisy background
Vortex collision cell provides efficient dissociation of ions in the cell, improved focusing and transmission of ions, and rapid clearance of the cell between mass transitions, thereby allowing for more MRMs/sec, zero crosstalk, and greater confidence in results by removing noisy background
Intuitive 'Quant-My-Way' software and the MassHunter Productivity App boost productivity by up to 40%, require less need for operator training, reduce time spent reviewing data, and simplify report generation
Enhanced maintenance feedback (EMF) features deliver smart, self-aware diagnostics to ensure optimum uptime and help drive down maintenance costs
Built-in technical controls combined with procedural controls ensure the security of your data, control access, and facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11 and similar national electronic record regulations