MStern Blotting–High Throughput Polyvinylidene Fluoride (PVDF) Membrane-Based Proteomic Sample Preparation for 96-Well Plates * [S]
Molecular & Cellular Proteomics, ISSN: 1535-9476, Vol: 14, Issue: 10, Page: 2814-2823
2015
- 65Citations
- 109Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations65
- Citation Indexes65
- 65
- CrossRef34
- Captures109
- Readers109
- 109
Article Description
We describe a 96-well plate compatible membrane-based proteomic sample processing method, which enables the complete processing of 96 samples (or multiples thereof) within a single workday. This method uses a large-pore hydrophobic PVDF membrane that efficiently adsorbs proteins, resulting in fast liquid transfer through the membrane and significantly reduced sample processing times. Low liquid transfer speeds have prevented the useful 96-well plate implementation of FASP as a widely used membrane-based proteomic sample processing method. We validated our approach on whole-cell lysate and urine and cerebrospinal fluid as clinically relevant body fluids. Without compromising peptide and protein identification, our method uses a vacuum manifold and circumvents the need for digest desalting, making our processing method compatible with standard liquid handling robots. In summary, our new method maintains the strengths of FASP and simultaneously overcomes one of the major limitations of FASP without compromising protein identification and quantification.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1535947620326347; http://dx.doi.org/10.1074/mcp.o115.049650; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84942872039&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26223766; https://linkinghub.elsevier.com/retrieve/pii/S1535947620326347; http://www.mcponline.org/lookup/doi/10.1074/mcp.O115.049650; https://syndication.highwire.org/content/doi/10.1074/mcp.O115.049650; https://dx.doi.org/10.1074/mcp.o115.049650
Elsevier BV
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