The phrase "amplification targets" is correct and usable in written English.
It can be used in contexts related to biology, genetics, or any field where specific targets for amplification processes are discussed, such as PCR (Polymerase Chain Reaction).
Example: "In our experiment, we identified several amplification targets that will enhance the accuracy of our results."
Alternatives: "amplification objectives" or "amplification endpoints".
The APGC program was applied to identify amplification targets for improving production, and OptGeneKnock and IdealKnock were used to identify knockout targets.
Consequently, poor design combined with failure to optimise reaction conditions is likely to result in reduced technical precision and false positive or negative detection of amplification targets.
The targets were chosen to provide quantification and fragment length information relevant to the STR amplification targets commonly used for forensic genotyping.
In addition, 6 gene amplification targets were predicted by APGC framework, which could lead to a 34.1% improvement of TAG production for increasing the availability of important precursors of acetyl-CoA and malonyl-CoA.
Comparative analysis of 24 M. haemolytica genomes was used to identify unique genes associated with capsular polysaccharide synthesis as amplification targets in a multiplex PCR assay to discriminate between serotype 1, 2, and 6 strains.
Herein, we first investigated the coupled relationship of growth and production, and subsequently proposed an algorithm, called analysis of production and growth coupling (APGC), to identify amplification targets for improving production of the desired metabolite.
We investigated both on the choice of the amplification target, and on the matrix effect on different sample foods.
Furthermore, we speculated reaction NADH16, the conversion of ubiquinone-8 (q8) to ubiquinol-8 (q8h2), as a potential amplification target for anaerobically improving cell growth and succinate production in NZN111.
The yield, purity and quality of DNA was measured and used for PCR amplification targeting V2 V3 region of eubacterial 16S rRNA gene.
We present data validating a real-time PCR assay quantifying P. vivax parasitemia, using the small subunit ribosomal RNA genes as an amplification target.
Study design: HEV RNA sequences were obtained from the GenBank database and the software dnasis was used to predict the presence of secondary structures within the amplification target regions.
