2007
DOI: 10.1016/j.jbbm.2006.11.008
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Usefulness of the 5′ region of the cDNA encoding acidic ribosomal phosphoprotein P0 conserved among rats, mice, and humans as a standard probe for gene expression analysis in different tissues and animal species

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Cited by 108 publications
(85 citation statements)
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“…Q-PCR is most economical, versatile, less time consuming and highly sensitive method, which generates a T/S ratio that is proportional to a cell's average telomere length. We used single copy acidic ribosomal phosphoprotein P0 expressing 36B4 gene to compare the telomere repeat sequence, because, its cDNA nucleotide sequence has highly conserved in the 5-prime end of its open reading frame among the tissues and species making it as most preferred reference gene [30].…”
Section: Discussionmentioning
confidence: 99%
“…Q-PCR is most economical, versatile, less time consuming and highly sensitive method, which generates a T/S ratio that is proportional to a cell's average telomere length. We used single copy acidic ribosomal phosphoprotein P0 expressing 36B4 gene to compare the telomere repeat sequence, because, its cDNA nucleotide sequence has highly conserved in the 5-prime end of its open reading frame among the tissues and species making it as most preferred reference gene [30].…”
Section: Discussionmentioning
confidence: 99%
“…All reactions were performed with Power SyBR ® Green Master Mix (Applied Biosystems) according to manufacturer's instructions. The relative amount of transcripts was calculated using comparative C T method and Acidic Ribosomal Phosphoprotein P0 mRNA was used for normalization [13].…”
Section: Atp Measurementmentioning
confidence: 99%
“…Products were amplified on Applied Biosystems 7500 Real-Time PCR System (Life Technologies Co.) using iQ SYBR Green Supermix. Cycle parameters were 50 8C for 2 min and 95 8C for 10 min, followed by 44 cycles at 95 8C for 15 s, 53 8C for 30 s, and 72 8C for 45 s. The intron spanning primers used in this manuscript have been described earlier by our own group and by others (Rodgers et al 2005, Akamine et al 2007, Machado et al 2009, Paula et al 2010, 2012, Santiago et al 2011. Efficiency of each reaction was calculated using a serial dilution and varied from 94% for SIRT1 to 98% for 36B4, and products' purity was confirmed by agarose gel analysis.…”
Section: Animal Care and Treatmentsmentioning
confidence: 99%