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Proteomics PDF Print E-mail
Written by malva   
Thursday, 12 February 2009 22:45


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Waters is a leading resource for the delivery of tailored analytical solutions to meet the demands of leading proteomics and biomarker discovery research laboratories. Building on more than 30 years of experience, our advanced mass spectrometry systems maximize efficiency and provide unique tools for protein discovery, characterization, quantification, and validation.

 

Integrated Bioinformatics

  • Work in a complete proteome analysis environment with ProteinLynx Global SERVER platform for data processing, protein identification, quantification, and characterization project/sample management, MASCOT integration and IBM eSERVER solutions.
  • Support for a variety of data formats such as XML and m/z data plus formats for third-party search engines like SEQUEST, DTA, and MASCOT, PKL.

The Identity[E] High Definition Proteomics System, for qualitative protein identification, enables proteomics researchers to use a simple routine to determine absolute protein concentrations.
Protein Quantification
The Expression[E] High Definition Proteomics System quantitatively and qualitatively maps complex biological digests for multiplexed protein expression profiling and biomarker research.
Waters Verify[E] System for hypothesis-driven proteomics augments Waters High Definition Proteomics Strategy, complementing global-discovery proteomics systems: Identity[E] and Expression[E].
Take advantage of powerful and versatile, analytical- to capillary-scale HPLC and UPLC systems for peptide separation, protein pre-fractionation, and protein purification.
Combine UPLC technology with MALDI time-of-flight mass spectrometry for the highest confidence in de novo peptide sequencing and BLAST analyses, post-translational moditication identification, and PTM characterization.
The direct profiling of tissue sections by MALDI mass spectrometry, using molecular imaging, is a powerful complement to existing methods of biomarker discovery.
Last Updated on Wednesday, 18 February 2009 11:25