Reference gene selections for real time quantitative PCR analysis of gene expression in different oat tissues and under salt stress
Author:
Publisher
Institute of Experimental Botany
Subject
Horticulture,Plant Science
Link
http://bp.ueb.cas.cz/doi/10.32615/bp.2020.153.pdf
Reference28 articles.
1. Assessment of reference genes for real-time quantitative PCR normalization in Ilex paraguariensis leaves during drought
2. Normalization of Real-Time Quantitative Reverse Transcription-PCR Data: A Model-Based Variance Estimation Approach to Identify Genes Suited for Normalization, Applied to Bladder and Colon Cancer Data Sets
3. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays
4. Normalization of qRT-PCR data: the necessity of adopting a systematic, experimental conditions-specific, validation of references
5. RefGenes: identification of reliable and condition specific reference genes for RT-qPCR data normalization
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1. Genome-Wide Identification of NAC Family Genes in Oat and Functional Characterization of AsNAC109 in Abiotic Stress Tolerance;Plants;2024-04-03
2. Selection and Validation of Reference Genes in Sudan Grass (Sorghum sudanense (Piper) Stapf) under Various Abiotic Stresses by qRT-PCR;Genes;2024-02-06
3. Cross-Species Evaluation of qPCR Reference Genes inDiabrotica speciosa(Coleoptera: Chrysomelidae) using Diabrotica virgifera virgifera sequences;2023-12-07
4. Genome-Wide Identification of Nac Family Genes in Common Oat (Avena Sativa L.) and Functional Characterization of Asnac109 in Abiotic Stress Tolerance;2023
5. Reference genes expression stability in Avena sativa L. during compatible and incompatible interactions with Puccinia graminis;Scientific Reports;2022-11-01
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