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The content of the specified constituent must be determined by quantitative analysis.
The comonomer composition of the resulting poly(oxy-1-chloromethylethylene-co-oxy-1-phenoxymethyl-ethylene-co-oxy-1-methyleneethylene) can be determined by quantitative 13C nuclear magnetic resonance (n.m.r).
The expression of a selection of a smaller number of miRNAs can be determined by quantitative real-time RT-PCR.
However, the relative expression levels of both splice variants could be determined by quantitative real-time RT-PCR.
By employing this method, only few transformants survive on high concentrations of antibiotic, but will most likely contain multiple copies, which can be determined by quantitative (qPCR) or Southern blot analysis (M. Ahmad, unpublished results).
The relative expression levels of both splice variants of efg8 could not be determined by quantitative real-time RT-PCR because non-specific side products defeated the analysis repeatedly (the same was true for mgmt, nrnp1 and selEFf).
Similar(53)
Serum HIV RNA levels were determined by quantitative PCR.
Using these DNA samples, the concentration of proviral DNA was determined by quantitative PCR.
mRNA expression levels of indicated genes were determined by quantitative reverse trancriptase PCR in population doublings, PD10 and PD55 IMR90 cells.
Gene expression levels were determined by quantitative PCR reactions (ABI 7500) in the presence of SYBR Premix ExTaq (Takara Bio) fluorescent dye.
The concentration of proinflammatory cytokines and chemokines in CVL was determined by quantitative ELISA.
More suggestions(15)
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