Shanghai Genstech Technology Co.,Ltd

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    Primer Synthesis Industry

    Summar

    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

    Summar

    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

    Summar

    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

    Summar

    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

    Summar

    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

    Summar

    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