Laser-Capture Microdissection of Renal Tubule Cells and Linear Amplification of RNA for Microarray Profiling and Real-Time PCR
Methods in Molecular Biology, ISSN: 1940-6029, Vol: 755, Page: 257-266
2011
- 5Citations
- 12Captures
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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.
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Metrics Details
- Citations5
- Citation Indexes5
- CrossRef3
- Captures12
- Readers12
- 12
Book Chapter Description
Laser-capture microdissection and transcriptional profiling have enabled compartment- and cell-specific analysis of gene expression in chronic kidney disease, thus facilitating the investigation of pathophysiological associations between glomerular, tubular, and interstitial structures. Due to the pico- and nanogram amounts of RNA isolated from LCM-captured material linear RNA amplification protocols are necessary prior to real-time PCR and microarray analysis. In this chapter, we describe the isolation of renal tubule cells from cryocut sections from routine kidney biopsies, and the isolation and linear amplification of RNA for downstream purposes.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79960945112&origin=inward; http://dx.doi.org/10.1007/978-1-61779-163-5_21; http://www.ncbi.nlm.nih.gov/pubmed/21761310; https://link.springer.com/10.1007/978-1-61779-163-5_21; http://www.springerlink.com/index/10.1007/978-1-61779-163-5_21; http://www.springerlink.com/index/pdf/10.1007/978-1-61779-163-5_21; https://dx.doi.org/10.1007/978-1-61779-163-5_21; https://link.springer.com/protocol/10.1007/978-1-61779-163-5_21
Springer Science and Business Media LLC
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