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The mtDNA copy number was determined using a competitive polymerase chain reaction (PCR) method (Lee et al, 1998, 2004).
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In this report the expression of the ubiquitin-proteasome pathway in rectus abdominis muscle has been determined in cancer patients with weight loss of 0 34% using a competitive reverse transcriptase polymerase chain reaction to measure expression of mRNA for proteasome subunits C2 and C5, while protein expression has been determined by western blotting.
Genotyping was performed by using a competitive allele-specific polymerase chain reaction system (KASpar genotyping; KBioscience, Hoddesdon, UK).
IgG against BTV was detected by using a competitive ELISA (Pourquier Bluetongue Competitive ELISA; Pourquier Laboratory, Montpellier, France).
We devised and verified such a tool using a quantitative competitive polymerase chain reaction approach.
In this study, we describe a competitive polymerase chain reaction (PCR) for the quantification of the sequences of dsrAB in sulfate-reducing microorganisms.
We first used a competitive binding assay.
Statistical tests conducted use a competitive null hypothesis.
HPV status was determined by an ultrasensitive method using real-time competitive polymerase chain reaction (PCR) and matrix-assisted laser desorption/ionization mass spectroscopy, as described in Tang et al. [ 35].
HPV status was determined by an ultra-sensitive method using real-time competitive polymerase chain reaction and matrix-assisted laser desorption/ionization-time of flight mass spectroscopy with separation of products on a matrix-loaded silicon chip array.
A link between breast cancer and local estrogen biosynthesis suggested by quantification of breast adipose tissue aromatase cytochrome P450 transcripts using competitive polymerase chain reaction after reverse transcription.
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