<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">PAR</journal-id><journal-title-group><journal-title>Proceedings of Anticancer Research</journal-title></journal-title-group><issn>2208-3545</issn><eissn>2208-3553</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/par.v5i4.2239</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>The Effect of Elution Volume for Immunoprecipitation on m6A-Seq Analysis</title><url>https://artdesignp.com/journal/PAR/5/4/10.26689/par.v5i4.2239</url><author>XuYuhui,ShenLize,LiGuolin</author><pub-date pub-type="publication-year"><year>2021</year></pub-date><volume>5</volume><issue>4</issue><history><date date-type="pub"><published-time>2021-07-29</published-time></date></history><abstract>Objective: To develop a cost-effective method to reduce the time consumption of elution in immunoprecipitation. Method: Two volumes (125 ?L for Group C and 100 ?L for Group T) of elution buffer were used to explore whether smaller volume could save testing time. Result: Time consumption of elution in Group T was significantly shorter than that in Group C, while the efficiency of eluted m6A-containing fragments and the performance of m6A-Seq as indicated by m6A peak distributions showed no difference between the two groups. Conclusion: A smaller volume of elution buffer was an economical way to reduce time consumption in immunoprecipitation.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Jiang XL, Liu BY, Nie Z, et al., 2021, The Role of m6A Modification in the Biological Functions and Diseases. Signal Transduction and Targeted Therapy, 6(1): 74.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Meyer KD, Saletore Y, Zumbo P, et al., 2012, Comprehensive Analysis of MRNA Methylation Reveals Enrichment in 3’ UTRS and Near Stop Codons. Cell, 149(7): 1635-1646.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B3" content-type="article"><label>3</label><element-citation publication-type="journal"><p>Dominissini D, Moshkovitz S, Schwartz, et al., 2012, Topology of the Human and Mouse m6a RNA Methylomes Revealed by m6a-Seq. Nature, 485(7397): 201-206.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
