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Publicação:
Bona fide gene expression analysis of samples from the bovine reproductive system by microfluidic platform

dc.contributor.authorFontes, Patricia Kubo [UNESP]
dc.contributor.authorCastilho, Anthony César Souza [UNESP]
dc.contributor.authorRazza, Eduardo Montanari [UNESP]
dc.contributor.authorNogueira, Marcelo Fábio Gouveia [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Western São Paulo (Unoeste)
dc.date.accessioned2020-12-12T01:57:11Z
dc.date.available2020-12-12T01:57:11Z
dc.date.issued2020-05-01
dc.description.abstractSample types such as those from reproductive systems often yield scarce material, which limits RT-qPCR analysis to only a few targets. Recently developed high-throughput systems can potentially change this scenario, however, the nanoliter scale of such platforms requires extra processing, e.g., preamplification, which needs to be defined through observation and experience. In order to establish best practices in high-throughput PCR approaches using samples from reproductive systems, we evaluated the Biomark™ HD performance using 11 different sample types from the bovine reproductive system: blastocyst (single/pool), oocyte (pool), cumulus, granulosa, and theca cells, oviduct tissue, fetal ovary, testicle (adult/fetal), and uterine horn. We observed that the preamplification step is not just reliable, but mandatory. Our results indicated that 14-preamplification cycles associated to 5- and 7-fold-dilution is the best approach for those samples. Additionally, the Biomark™ HD system has a high intra and inter reproducibility, therefore its performance in duplicate is unnecessary for the ΔCq analysis, taking in consideration the cutoff value 4 < Cq < 22. In summary, this high-throughput approach is a reliable and excellent tool for studying the bovine reproductive system, especially using quantitatively-limited samples, as a larger number of target genes can be assessed from a very low amount of starting material.en
dc.description.affiliationLaboratory of Phytomedicines Pharmacology and Biotechnology Department of Pharmacology Institute of Biosciences University of São Paulo State (Unesp) Campus of Botucatu, São Paulo
dc.description.affiliationUniversity of Western São Paulo (Unoeste) Campus of Presidente Prudente, São Paulo
dc.description.affiliationDepartment of Biological Sciences School of Sciences and Languages São Paulo State University (Unesp) Campus of Assis, São Paulo
dc.description.affiliationUnespLaboratory of Phytomedicines Pharmacology and Biotechnology Department of Pharmacology Institute of Biosciences University of São Paulo State (Unesp) Campus of Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Biological Sciences School of Sciences and Languages São Paulo State University (Unesp) Campus of Assis, São Paulo
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2012/50533–2
dc.identifierhttp://dx.doi.org/10.1016/j.ab.2020.113641
dc.identifier.citationAnalytical Biochemistry, v. 596.
dc.identifier.doi10.1016/j.ab.2020.113641
dc.identifier.issn1096-0309
dc.identifier.issn0003-2697
dc.identifier.scopus2-s2.0-85079657707
dc.identifier.urihttp://hdl.handle.net/11449/200080
dc.language.isoeng
dc.relation.ispartofAnalytical Biochemistry
dc.sourceScopus
dc.subjectGene expression
dc.subjectHigh-throughput qPCR system
dc.subjectLow RNA concentration
dc.subjectMicrofluids
dc.subjectPreamplification
dc.subjectReproductive system
dc.titleBona fide gene expression analysis of samples from the bovine reproductive system by microfluidic platformen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentCiências Biológicas - FCLASpt
unesp.departmentFarmacologia - IBBpt

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