污渍
规范化(社会学)
免疫印迹
生物
蛋白质表达
定量蛋白质组学
细胞外小泡
蛋白质组学
甘油醛3-磷酸脱氢酶
分子生物学
细胞生物学
生物化学
信使核糖核酸
基因
社会学
人类学
作者
Anjugam Paramanantham,Rahmat Asfiya,Siddharth Das,Grace McCully,Akhil Srivastava
标识
DOI:10.1080/10826068.2023.2185897
摘要
Western blot analysis of relative protein expression relies on appropriate reference proteins for data normalization. Small extracellular vesicles (sEVs), or exosomes, are increasingly recognized as potential indicators of the physiological state of cells due to their protein composition. Therefore, accurate relative sEVs protein quantification is crucial for disease detection and prognosis applications. Currently, no documented ubiquitous reference proteins are identified for precise normalization of a protein of interest in sEVs. Here we showed the use of total protein staining method for sEVs protein normalization in western blots of samples where conventional housekeeping proteins like β-actin and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) are not always detected in the sEVs western blots. The No-Stain™ Protein Labeling (NSPL) method showed high sensitivity in sEVs-protein labeling and facilitated quantitative evaluation of changes in the expression pattern of the protein of interest. Further, to show the robustness of NSPL for expression analysis, the results were compared with quantitative mass spectroscopy analysis results. Here, we outline a comprehensive method for protein normalization in sEVs that will increase the value of protein expression study of therapeutically significant sEVs.
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