Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.
The separation and quantification of major milk proteins is fundamental in dairy research. Therefore, accurate and rapid methods
are profoundly important. The microfluidic chip technique is faster, and uses considerably fewer chemicals and materials than
traditional techniques. The objective of this study was to improve experimental methods for separating and quantifying major milk
proteins using the microfluidic chip technique. Deionized water, a total protein solubilization buffer (TPS buffer) and a separating
milk protein buffer (SEP buffer) were added for the treatment of milk samples and their effects were evaluated. The results showed an
excellent separation for whey proteins with �±-lactalbumin migrating first, followed by �²-lactoglobulin in the presence of both buffers.
However, better results for major casein separation were achieved when the SEP buffer was added. The order of the migration time
was: �²-casein first, followed by �±s-casein and �º-casein. The quantitative analysis showed significant differences among the percentages
of protein fractions from both buffers. The results using microfluidic chip technology using the SEP buffer solution were comparable
to those obtained by SDS-PAGE for these proteins and with the data reported in the literature.