[HTML][HTML] Evaluation of appropriate reference genes for reverse transcription-quantitative PCR studies in different tissues of a desert poplar via comparision of different …

HL Wang, L Li, S Tang, C Yuan, Q Tian, Y Su… - International journal of …, 2015 - mdpi.com
Despite the unshakable status of reverse transcription-quantitative PCR in gene expression
analysis, it has certain disadvantages, including that the results are highly dependent on the …

[HTML][HTML] Reference Gene Selection for Quantitative Real-time PCR Normalization in Caragana intermedia under Different Abiotic Stress Conditions

J Zhu, L Zhang, W Li, S Han, W Yang, L Qi - PloS one, 2013 - journals.plos.org
Quantitative real-time reverse transcription polymerase chain reaction (qPCR), a sensitive
technique for gene expression analysis, depends on the stability of the reference genes …

[HTML][HTML] Selection and identification of a reference gene for normalizing real-time PCR in mangos under various stimuli in different tissues

R Yao, X Huang, H Cong, F Qiao, Y Cheng, Y Chen - Horticulturae, 2022 - mdpi.com
Real-time quantitative polymerase chain reaction (Real-Time PCR) is a rapid, highly
sensitive, and highly specific technique, which is widely used to determine the relative …

Selection and Validation of Reference Genes for RT‐qPCR Analysis in Spinacia oleracea under Abiotic Stress

H Xie, B Li, Y Chang, X Hou, Y Zhang… - BioMed Research …, 2021 - Wiley Online Library
Reverse transcription quantitative real‐time polymerase chain reaction (RT‐qPCR) is an
accurate and convenient method for mRNA quantification. Selection of optimal reference …

[PDF][PDF] Reference gene selections for real time quantitative PCR analysis of gene expression in different oat tissues and under salt stress.

ZL Duan, WH Han, L Yan, B Wu - Biologia plantarum, 2020 - bp.ueb.cas.cz
Appropriate choice of reference genes for data normalization is of critical importance for
accurate real time reverse transcription quantitative PCR (RT-qPCR) analysis of gene …

Identification of suitable reference genes for normalization of real-time quantitative PCR data in pecan (Carya illinoinensis)

Z Mo, Y Chen, W Lou, X Jia, M Zhai, J Xuan, Z Guo… - Trees, 2020 - Springer
Key message This study proposed the combination of PR26S and PP1 as a good choice for
RT-qPCR normalization in pecan under abiotic stress, developing kernels, grafting, and …

[HTML][HTML] Stable internal reference genes for the normalization of real-time PCR in different sweetpotato cultivars subjected to abiotic stress conditions

SC Park, YH Kim, CY Ji, S Park, JC Jeong, HS Lee… - PloS one, 2012 - journals.plos.org
Reverse transcription quantitative real-time PCR (RT-qPCR) has become one of the most
widely used methods for gene expression analysis, but its successful application depends …

[HTML][HTML] Reference Gene Selection for Quantitative Real-Time PCR Normalization in Reaumuria soongorica

X Yan, X Dong, W Zhang, H Yin, H Xiao, P Chen… - PloS one, 2014 - journals.plos.org
Despite its superiority for evaluating gene expression, real-time quantitative polymerase
chain reaction (qPCR) results can be significantly biased by the use of inappropriate …

[HTML][HTML] Selection of Suitable Reference Genes for RT-qPCR Normalization under Abiotic Stresses and Hormone Stimulation in Persimmon (Diospyros kaki Thunb)

P Wang, A Xiong, Z Gao, X Yu, M Li, Y Hou, C Sun… - PloS one, 2016 - journals.plos.org
The success of quantitative real-time reverse transcription polymerase chain reaction (RT-
qPCR) to quantify gene expression depends on the stability of the reference genes used for …

[HTML][HTML] Screening and Validation of Appropriate Reference Genes for Real-Time Quantitative PCR under PEG, NaCl and ZnSO4 Treatments in Broussonetia …

M Chen, Z Wang, Z Hao, H Li, Q Feng, X Yang… - International Journal of …, 2023 - mdpi.com
Real-time quantitative PCR (RT-qPCR) has a high sensitivity and strong specificity, and is
widely used in the analysis of gene expression. Selecting appropriate internal reference …