Sentence examples for genomic polymerase from inspiring English sources

Recently, c-MYC amplification was observed as a significant poor-prognostic factor by using whole genome copy number analysis and real-time genomic polymerase chain reaction (RT-G-PCR) in small-sized or early stage lung adenocarcinoma (Iwakawa et al, 2011).

In one putative female strain, the female-specific gene HMG1f was not amplified by genomic polymerase chain reaction.

Genomic polymerase chain reaction (PCR) using primers specific for the T-DNA integration site confirmed the homozygous status of the plants (Figure 1b), while primers specific for exon 3 were used to check the quality of the DNA (Figure 1c).

We performed genomic polymerase chain reaction (PCR) using the primers listed in Table 2 to check the presence or absence of several sex-specific genes and the sex-based divergent genes MAT3m, MAT3f and LEU1Sm (Ferris et al. 2010) in the 33 Taiwanese strains and Eve.

PCR screening was performed with the Advantage GC genomic polymerase (Clontech, Mountain View, CA).

ABCG2 polymorphism (−15662C/T) was genotyped using genomic polymerase chain reaction (PCR) and direct sequencing.

In this way a plausible pathway from simple oligonucleotide replicators to genomic polymerases can be imagined, as can a pathway from basal ribozyme activities to the ribosome.

Quantitative-genomic polymerase chain reaction (Q-PCR) was performed to quantify PRL-3 gene copy numbers using iQ™ Supermix (Bio-Rad Laboratories, HerCAles, CA) in triplicate on the iCycler iQ™ Real-Time PCR Detection system (Bio-Rad).

General molecular biology techniques including isolation of genomic DNA, polymerase chain reactions (PCR), restriction enzyme digestion and ligation, electroporation, Southern hybridization, Western analysis, etc were performed as described earlier [49].

Reaction tubes contained genomic DNA, polymerase buffer, 0.25  μM of each primer (forward flanking, reverse flanking primer, and ASO-primer) (Sigma-Aldrich), 0.5  μM dNTPs, 1.5  μM MgCl2, 1 U/ μL polymerase (BIOTOOLS B&M Labs), and H2O.

The possibility of misplaced DNA sequences in the genomic database, polymerase chain reaction mispriming, contamination, incomplete sequence data, and poorly rooted trees can also be technical sources of errors for HT detection (Lisch 2008).