Literature DB >> 22144198

MicroRNA profiling using µParaflo microfluidic array technology.

Xiaochuan Zhou1, Qi Zhu, Christoph Eicken, Nijing Sheng, Xiaolin Zhang, Litao Yang, Xiaolian Gao.   

Abstract

The diverse functions of microRNA (miRNA) molecules have drawn broad and intensive interest in various biological fields, biomedical applications, and technology development. Which are endogeneous cellular short RNA molecules found in the cytoplasm as well as in various serum fluids. miRNAs are transcriptional and translational regulatory molecules active in cell division, growth, and apoptosis (1). Dysregulated expression of miRNAs has been implicated in various disease states and has been tested as biomarker candidates (2-4). miRNAs are endogeneous cellular short RNA molecules found in the cytoplasm as well as in various serum fluids. miRNAs are transcriptional and translational regulatory molecules active in cell division, growth, and apoptosis (Bartel, Cell 116:281-97, 2004). Dysregulated expression of miRNAs has been implicated in various disease states and has been tested as biomarker candidates (He et al., Nature 435:828-833, 2005; Lu et al., Nature 435:834-838, 2005; O'Donnell, et al., Nature 435:839-843, 2005). In this chapter, we describe the methods using μParaflo(®) microfluidic oligonucleotide microarray technology for applications in miRNA profiling. One unique feature of this technology is the flexibility that provides users with the freedom to select sequence content either for focused studies wherein only the most relevant sequences are included or for discovery studies wherein the most updated sequence content such as those newly derived from deep sequencing. This chapter provides detailed information from experimental design to sample preparation, as well as data analysis for a miRNA array experiment.

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Year:  2012        PMID: 22144198     DOI: 10.1007/978-1-61779-427-8_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  MicroRNAs are Necessary for BMP-7-induced Dendritic Growth in Cultured Rat Sympathetic Neurons.

Authors:  Kristina Pravoverov; Katherine Whiting; Slesha Thapa; Trevor Bushong; Karen Trang; Pamela J Lein; Vidya Chandrasekaran
Journal:  Cell Mol Neurobiol       Date:  2019-05-18       Impact factor: 5.046

Review 2.  Microfluidic epigenomic mapping technologies for precision medicine.

Authors:  Chengyu Deng; Lynette B Naler; Chang Lu
Journal:  Lab Chip       Date:  2019-07-24       Impact factor: 6.799

Review 3.  Potential pitfalls in microRNA profiling.

Authors:  Pauline Chugh; Dirk P Dittmer
Journal:  Wiley Interdiscip Rev RNA       Date:  2012-05-07       Impact factor: 9.957

4.  Expression Profiles of Estrogen-Regulated MicroRNAs in Breast Cancer Cells.

Authors:  Anne Katchy; Cecilia Williams
Journal:  Methods Mol Biol       Date:  2016

5.  Expression Profiles of Estrogen-Regulated MicroRNAs in Cancer Cells.

Authors:  Amena Archer; Claudia Kutter; Cecilia Williams
Journal:  Methods Mol Biol       Date:  2022

6.  Profiling of estrogen-regulated microRNAs in breast cancer cells.

Authors:  Anne Katchy; Cecilia Williams
Journal:  J Vis Exp       Date:  2014-02-21       Impact factor: 1.355

7.  Rapid identification of ubiquitination and SUMOylation target sites by microfluidic peptide array.

Authors:  Bing Zhu; Tierra R Farris; Sarah L Milligan; Haosi Chen; Ruijuan Zhu; Aailing Hong; Xiaochuan Zhou; Xiaolian Gao; Jere W McBride
Journal:  Biochem Biophys Rep       Date:  2016-03-01
  7 in total

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