SILAC analysis
2 RESULTS
shirley, NY USA, Accord
SILAC-based quantitative proteomics (SILAQ) is an innovative technology used in high throughput quantitative analysis of large protein complexes protein-protein and protein-small molecule interactions. SILAC service of Creative Proteomics provides an unbiased strategy that can reveal how specifically either inhibitors or other perturbations affect the dynamic properties and cellular distributions of proteins. It can also be used as a sensitive and effective method to determine the specific interaction partners of proteins in the cell.... read more
SILAC-based quantitative proteomics (SILAQ) is an innovative technology used in high throughput quantitative analysis of large protein complexes protein-protein and protein-small molecule interactions. SILAC service of Creative Proteomics provides an unbiased strategy that can reveal how specifically either inhibitors or other perturbations affect the dynamic properties and cellular distributions of proteins. It can also be used as a sensitive and effective method to determine the specific interaction partners of proteins in the cell.... read more
shirley, NY USA, Accord
Tel: 1782281233
Stable isotope labeling by amino acids in cell culture (SILAC) is a powerful method to study the relative proteomic change under differential treatments which relies on the mass spectrometry and the metabolic incorporation of amino acids with substituted stable isotopic nuclei. In SILAC a given 'light' or 'heavy' form of the amino acid is incorporated into two samples. Two cell populations are grown in culture media that are identical except that one of them contains a 'light' and the other contains a 'heavy' form of a particular amino acid (e.g. 12C and 13C labeled L-lysine respectively). As the two isotopically... read more
Tel: 1782281233
Stable isotope labeling by amino acids in cell culture (SILAC) is a powerful method to study the relative proteomic change under differential treatments which relies on the mass spectrometry and the metabolic incorporation of amino acids with substituted stable isotopic nuclei. In SILAC a given 'light' or 'heavy' form of the amino acid is incorporated into two samples. Two cell populations are grown in culture media that are identical except that one of them contains a 'light' and the other contains a 'heavy' form of a particular amino acid (e.g. 12C and 13C labeled L-lysine respectively). As the two isotopically... read more
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