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In addition, the improvements of purification, enrichment and fractionation will be great helpful for the characterization and quantitation of glycoproteins.
Liquid chromatography coupled with mass spectrometry (LC-MS) has become the method of choice for the characterization and quantitation of covalent modification of DNA in various biological samples.
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Proteomics, or protein pattern analysis, is the characterization and quantitation of proteins in tissues and body fluids [ 5].
Liquid chromatography mass spectrometry (LC MS) is currently the primary method for characterization and quantitation of covalent modification of DNA, commonly performed using tandem mass spectrometry and positive mode electrospray ionization.
The currently used analytical methods for identification, characterization and quantitation of asbestos fiber in consumer talcum products include polarized light microscopy, x-ray diffraction analysis, transmission electron microscopy with selected area electron diffraction and electron microprobe techniques.
Furthermore, this study demonstrates the first characterization and quantitation of DNA phosphate adducts of the tobacco-specific nitrosamines and provides chemical support for using phosphate adducts as potential biomarkers to investigate tobacco exposure and associated cancer risk.
Mass spectrometry-based proteomics is an effective tool for protein identification, characterization, and quantitation.
The remaining cells were used for lipid isolation and quantitation of cholesterol concentration using the colorometric Cholesterol/Cholesteryl Ester Quantitation Kit (Calbiochem).
Biosensors for detection and quantitation of lead (Pb) in water and blood serum are highly desired.
Soluble and alginate immobilized urease was utilized for detection and quantitation of mercury in aqueous samples.
In addition, it provides examples for detection and quantitation of environmental samples using QCM immunosensors.
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