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    <subfield code="a">Analysis of Protein Changes Using Two-Dimensional Difference Gel Electrophoresis</subfield>
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    <subfield code="v">Method Mol. Biol. Mol. Tox. Protocols, 1105, p.17-30, 2014</subfield>
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    <subfield code="a">A protocol for protein analysis using two-dimensional difference gel electrophoresis (2D-DIGE)is described. 2D-DIGE is one of the most popular and versatile methods of protein separation among rapidly increasing proteomics technologies. Similar to traditional two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), the proteins are separated based on their charges and molecular weight by 2D-DIGE. Different from 2D-PAGE, proteins are pre-labeled with different fl uorescent and different protein samples are run in one gel by this method. Therefore, 2D-DIGE not only carries the advantages of 2D-PAGE but also eliminates gel-to-gel variation and achieves high resolution, sensitivity, and reproducibility.</subfield>
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    <subfield code="a">TWO-DIMENSIONAL DIFFERENCE GEL ELECTROPHORESIS</subfield>
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    <subfield code="a">TWO-DIMENSIONAL POLYACRYLAMIDE GEL ELECTROPHORESIS</subfield>
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    <subfield code="a">PROTEIN SEPARATION</subfield>
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    <subfield code="a">Gao, W.</subfield>
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    <subfield code="z">Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx</subfield>
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    <subfield code="d">2025-06-25</subfield>
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    <subfield code="o">B-15038</subfield>
    <subfield code="r">2025-06-25 15:39:53</subfield>
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