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Primer Synthesis Industry

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Primer Customized Synthesis Industry

Preparation and purification

QC quality inspection

High-end research

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Analytical Preparative Purification
Industry characteristics: Most single preparations are less purified, and analytical grade purification schemes can be used.
Semi-Preparative Purification Platform
Suitable for large-volume preparation of nucleotides, single preparation amount up to 200~2000 OD
Quality Control
HTCS Nucleic Acid Mass Spectrometry Detection System (based on LTQ Series Mass Spectrometry) HTCS system based on Thermo LTQ mass spectrometry

Download link:Shanghai Genstech-Primer Synthesis Industry

RNA interference Industry Application Solutions

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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

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RNA interference Industry Quality Control
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
Thermo Q Exactive HRMS

Download link:Shanghai Genstecgh-RNA interference Industry

Small Molecule Pharmacy Industry Solution

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Small Molecule Pharmaceutical Industry1 -Small molecule method development/synthetic reaction monitoring/Quality certification (QA) and quality control (QC)/impurity analysis/small molecule preparation and purification

Small Molecule Pharmaceutical Industry 2- DMPK preclinical research and BE

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Small Molecule Pharmaceutical And Chemical Industry Ⅰ
Small molecule method development/synthetic reaction monitoring/Quality certification (QA) and quality control (QC)/impurity analysis/small molecule preparation and purification During the drug development process, method development will go through different stages, usually involving complex and variable samples. You need choose reliable and stable HPLC, UPLC, and GC to meet routine laboratory test
Small Molecule Pharmaceutical And Chemical Industry Ⅱ DMPK preclinical research
In the later development of drugs, quantitative bioanalysis using samples derived from PK research is an inevitable stage of drug development. Triple quadrupole is the product of choice and sensitivity is the most important indicator.
Small Molecule Pharmaceutical And Chemical Industry Ⅲ
Generic drug conformity assessment (BE) In vivo bioequivalence test (in vivo BE): Whether the bioequivalence between the generic drug and the original drug was significantly different by liquid chromatography tandem mass spectrometry. Bioequivalence refers to the fact that under similar conditions, the absorption rate and degree of the test preparation (T) after a single dose or multiple doses of the same amount of the drug component are not significantly different from the reference preparation (R).

Download link:Shanghai Gnestech-Small molecule pharmaceutical industry

Third Party Detection For Food And Environment

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HPLC, UPLC, GC, GCMS, LC-MS/MS 

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Triple Quadrupole LCMSMS For Quantification
A must-have requirement for third-party inspection industry---triple quadrupole mass spectrometry -LCMSMS
GC/GCMS for Qualitative And Quantification
The necessary requirements of the third-party testing industry----GC/GCMS
Quality Control
HTCS Nucleic Acid Mass Spectrometry Detection System (based on LTQ Series Mass Spectrometry) HTCS system based on Thermo LTQ mass spectrometry

Download link:Shanghai Genstech-Third Party Detection For

Monoclonal Antibody/Protein Industry

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Protein routine method development
protein preparation purification
protein amount control (biopharmaceutical characterization)
protein impurity analysis


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Mass Analysis Method Development
The most commonly used instrument in quality analysis laboratories-----HPLC,UPLC
Antibody Purification Pilot Test
GE ÄKTATM explorer Rapid process development liquid chromatography
Antibody Mass Analysis Structure Confirmation
Confirmation of Antibody Mass Analysis Structure--Beckman PA800
Antibody Impurity Analysis
The newest technology for antibody impurity analysis---based on multi-dimensional liquid chromatography and high resolution mass spectrometry for impurity identification

Download link:Shanghai Genstech-Monoclonal Antibody

Clinical Diagnosis

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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


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LCMSMS Clinical Mass Spectrometry
Instrument with medical registration license, with IVD logo (In Vitro Diagnostic)

Download link:Shanghai Gnestech-Clinical Diagnosis

Synthetic Peptide Solution

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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)

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Peptide Analysis(Regular Analysis
During the drug development process, method development will go through different stages, usually involving complex and variable samples. These work may waste money , time and repetitive work ,so you need to choose the most suitable HPLC system to work with.
Peptide Synthesis Reaction Monitoring
Synthetic Reaction Monitoring- Choose cost effective one New generation Waters UPLC+SQD LCMS
Peptide Analysis(High Resolution Mass Analysis)
Peptide accurate intact molecular weight determination Primary structure confirmation of peptide drugs (peptide mapping analysis) Peptide drug mass peptide map

Download link:Shanghai Genstech-Synthetic Polypeptide Industry