Dataset for the paper "Martín, Alba; Giráldez, F. Javier; Montero, O.; Andrés, S. 2022. Dietary administration of L-carnitine during the fattening period of early feed restricted lambs modifies liver transcriptomic and plasma metabolomic profiles. Animal Feed Science and Technology, 292:115426"

[Description of methods used for collection/generation of data] Liver samples stabilized in RNAlater were homogenized using RLT (Qiagen), Lysing Matrix D and a FastPrep-24 instrument (MP Biochemicals); RNA purification was performed with the RNeasy Mini kit and RNase-Free DNase Set kit (Qiagen). &qu...

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Detalles Bibliográficos
Autores: Andrés, Sonia, Giráldez, Francisco Javier, Martín González, Alba
Tipo de recurso: conjunto de datos
Fecha de publicación:2021
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/260397
Acceso en línea:http://hdl.handle.net/10261/260397
Access Level:acceso abierto
Palabra clave:Nutrional programming
Feed restriction
Feed efficiency
L-carnitine
Lamb
Liver
Transcriptomes
http://aims.fao.org/aos/agrovoc/c_92382
http://aims.fao.org/aos/agrovoc/c_4397
http://aims.fao.org/aos/agrovoc/c_7030
genómica
Ganado
Ovinos
Descripción
Sumario:[Description of methods used for collection/generation of data] Liver samples stabilized in RNAlater were homogenized using RLT (Qiagen), Lysing Matrix D and a FastPrep-24 instrument (MP Biochemicals); RNA purification was performed with the RNeasy Mini kit and RNase-Free DNase Set kit (Qiagen). "Poly(A)+ mRNA fraction was isolated from total RNA and cDNA libraries were obtained following Illumina´s recommendations. Briefly, poly(A)+ RNA was isolated on poly-T oligo-attached magnetic beads and chemically fragmented prior to reverse transcription and cDNA generation. The cDNA fragments then go through an end repair process, the addition of a single ‘A’ base to the 3’ end and then ligation of the adapters. Finally, the products are purified and enriched with PCR to create the indexed final double stranded cDNA library. The quality of the libraries was analyzed in Bioanalyzer 2100, High Sensitivity assay; the quantity of the libraries was determined by real-time PCR in LightCycler 480 (Roche). The pool of the libraries was sequenced by paired-end sequencing (100 × 2) in an Illumina HiSeq 2500 instrument."