2015
DOI: 10.1007/s10535-015-0501-6
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Cloning and characterization of four novel SnRK2 genes from Triticum polonicum

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Cited by 20 publications
(14 citation statements)
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“…Total RNA was isolated from the stems of DPW and HPW under photoperiod treatments, and genomic DNA was removed using an RNase-free DNase set (Omega) according to the user manual. The qPCR and data analysis were performed as described by Wang et al 64 . Ten differentially expressed genes from RNA-Seq were validated, and their primers are listed in Additional file 4 : Supplementary Table 1.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Total RNA was isolated from the stems of DPW and HPW under photoperiod treatments, and genomic DNA was removed using an RNase-free DNase set (Omega) according to the user manual. The qPCR and data analysis were performed as described by Wang et al 64 . Ten differentially expressed genes from RNA-Seq were validated, and their primers are listed in Additional file 4 : Supplementary Table 1.…”
Section: Methodsmentioning
confidence: 99%
“…Ten differentially expressed genes from RNA-Seq were validated, and their primers are listed in Additional file 4 : Supplementary Table 1. Actin, as described by Wang et al 64 , was used as a reference gene to normalize gene expression.…”
Section: Methodsmentioning
confidence: 99%
“…Quantitative real-time PCR with TpNRAMP3 -specific primers (forward: 5′-ACTCTGATGCTCCTGTTCCT-3′; reverse: 5′-GCCTCGCACAACTTCTGAA-3′) was performed as described by Wang et al (2015) with nine technological replicates of each sample. The actin gene ( Wang et al, 2015 ) was used as a reference gene to normalize relative expression level of TpNRAMP3 which was calculated by CFX Manager 3.1 (Bio-Rad, United States) using the 2 ΔΔ C t method.…”
Section: Methodsmentioning
confidence: 99%
“…Quantitative real-time PCR was performed on the CFX-96 system as described by Wang et al using a pair of Rht-B1b-speci c primers (forward: 5′-GGCGGGAGATCGAAGTAC-3′; reverse: 5′-GACACCGTGCACTACAAC-3′) [34]. To normalize gene expression levels, the Actin gene was used as the reference gene [34]. Relative expression levels were calculated according to the 2 ΔΔCt method using the CFX Manager (version 3.1; Bio-Rad, Hercules, CA, USA).…”
Section: Expression Analysis Of Rht-b1bmentioning
confidence: 99%