Laboratory technic for detecting and measuring a specific ADN sequence concentration.
1 MMP-3 expression was determined by enzyme-linked immunosorbent assay and quantitative polymerase chain reaction .
2 Differentially regulated transcripts were validated by reverse transcription- quantitative polymerase chain reaction .
3 The amplification was further validated with real-time quantitative polymerase chain reaction .
4 LTL was measured with a quantitative polymerase chain reaction method.
5 Gpr35 messenger RNA expression in cardiovascular tissues was assessed using quantitative polymerase chain reaction .
6 The lung tissue was characterized by histological and real-time quantitative polymerase chain reaction analysis.
7 Preferential upregulation of these plasma membrane-linked genes was validated by quantitative polymerase chain reaction .
8 Copy number analysis was measured by quantitative polymerase chain reaction and fluorescence in situ hybridization.
9 Cytokine gene expression in the urinary sediment was studied by real-time quantitative polymerase chain reaction .
10 These findings were verified by quantitative polymerase chain reaction .
11 The genotype and viral load of HPV were determined by fluorescence quantitative polymerase chain reaction .
12 Reverse transcription- quantitative polymerase chain reaction was used to validate the different expression levels of selected lncRNAs.
13 Reverse transcription- quantitative polymerase chain reaction was conducted to verify the candidate miRNAs discovered by microarray analysis.
14 Autophagy and apoptosis-related gene expression were assessed by real-time quantitative polymerase chain reaction and Western blot.
15 The expression of UASR1 in tissues and cells were detected by reverse transcription- quantitative polymerase chain reaction .
16 Real-time quantitative polymerase chain reaction evaluated RHOF expression in lymphocyte subpopulations, and normal and malignant lymphoid tissue.
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