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After an amplification process, the dPCR curves were statistically analyzed, and the quantification results were achieved without any working standards needed.
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The mixed ablation aerosols are analyzed and quantification is based on standard addition or isotope dilution.
Sequences were analyzed using the Quantification Tool for Methylation Analysis (QUMA, http://quma.cdb.riken.jp).jp
Sequence data were analyzed with the QUantification tool for Methylation Analysis (Kumaki et al., 2008).
JCS performed and analyzed the ABA quantification.
All of the membranes were analyzed by scanning densitometry and the quantification of bands was normalized using internal standards for each band.
By first amplifying the DNA sequence and then analyzing the product, quantification was exceedingly difficult since the PCR gave rise to essentially the same amount of product independently of the initial amount of DNA template molecules that were present.
To analyze the distribution and quantification of the key structural extracellular matrix components of the urethral tissue in a rat model of hyperglycemia and pregnancy.
Samples were withdrawn at different reaction times, centrifuged (14000 g, 10 min, 4°C), filtered (0.22 μm), and analyzed by HPLC for the quantification of CA and 4-VC.
Data were analyzed by the LightCycler quantification software to determine the threshold cycle above the background for each reaction.
The resulting data were analyzed by the relative quantification method using as calibrators either the low expressing control cells H441 or the parental monocytes (Fig. 1A and 1B).
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