Exact(60)
RNAseP was used as the reference gene.
Dissociation curves of the reference gene primers products.
The actin gene was used as the reference gene.
The reference gene used in this study was the RPLP0.
There is a strong correlation between the quality of the normalized data and the stability of the reference gene itself.
P. purpurogenum IAM15392 GAPDH was used as the reference gene for RT-PCR.
PCR efficiency analysis was performed to validate the optimal of the reference gene.
The expression level of EGFP was relative to ACTIN which acted as the reference gene.
Sorbonne polyubiquitin4 gene (GenBank accession no. DW718023) was used as the reference gene (Yamagishi 2011).
All wheat ESTs sharing high similarity with the reference gene were subjected to contig assembly.
G3PDH was chosen as the reference gene.
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