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Western blotting is a crucial technique for detecting specific target proteins in a sample. The process begins with SDS-PAGE, where proteins are denatured and negatively charged, allowing them to migrate through a gel towards a positively charged anode based on their molecular weight. After staining, distinct protein bands appear, with marker proteins serving as a reference for molecular weights. While an observed band may indicate the presence of a protein of interest, it does not confirm its identity, necessitating further analysis to determine the specific proteins present within that molecular weight range.