Primer Customized Synthesis Industry
Preparation and purification
QC quality inspection
High-end research
Quality Control Solution:
Uplc meet regulatory verification systems
Optimize the LC-MS workflow for quality control monitoring
Solvent residue monitoring
Heavy metal residue monitoring
RNA interference high-end research –HRMS for small nucleic acid drug characterization analysis
Small Molecule Pharmaceutical Industry 2- DMPK preclinical research and BE
HPLC, UPLC, GC, GCMS, LC-MS/MS
Protein routine method development
protein preparation purification
protein amount control (biopharmaceutical characterization)
protein impurity analysis
As a clinical diagnostic laboratory, it needs to be able to perform a large number of tests very accurately and sensitively, so it faces many difficulties. Current laboratory technology may be affected by cross reaction and result deviation. The supply of reagent kits available for new detection is slow, and sample preparation usually requires a lot of manual operations
The LC-MS/MS system for in vitro diagnosis is designed to help you optimize the entire laboratory workflow from pre-analysis (preparation of solution), analysis (LC to LC-MS/MS) to post-analysis (data information). With the continuous expansion of this product portfolio, the functions become more and more diverse, providing you with a large choice of LC-MS/MS for routine use in clinical laboratories
Synthetic peptide confirmation impurity analysis (HPLC/UPLC/LCMS)
Preparation and purification of synthetic peptides (Auto Prification)
Characterization of synthetic peptides and high-resolution impurity analysis (HRMS)