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  1. .... Contrary to earlier e- ports spurning the use of polyamines in PCR, ~12~ we determined that micromolar concentrations of spermidine nhanced PCR amplif ication significantly from plant DNA and that inclusion of spermi- dine to reactions was vastly superior to the compensatory effects of hot- start PCR...
  2. ...targeted genotyping of 45 inversions in 551 individuals by a combination of inverse PCR (iPCR) and multiplex ligation-dependent probe amplification (MLPA) (Giner-Delgado et al. 2019) has increased considerably the available human inversion data, although only IRs up to ∼25–30 kb could be spanned...
  3. ...RNAs were extracted and relative mRNA levels were determined by real-time PCR. Fabp4 mRNA was increased in the mature adipocytes (C) as well as both in the epidydimal white adipose tissue (epiWAT) and subcutaneous white adipose tissue (subWAT) of obese mice (D). Phb mRNA levels also increased in (E...
  4. ...and present hurdles to understanding the roles of mtDNA copy number variation during aging and disease onset and progression. This is at least in part due to the following: (1) the differing PCR amplification efficiency between the mtDNA target and housekeeping genes, leading to altered mtDNA/nDNA ratios...
  5. ...), elimination of exogenousDNA contaminationwith endonucleases (McrBC and DpnI), and minimization of the reaction volume (10 mL for initial amplification and 100 mL total). All manipulations were performed frombeginning to end in a single tube in a PCR chamber. In addition, this simple method is not labor...
  6. .... Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods Enzymol. 155 : 335 – 350 . 3. Erlich, H.A., ed. 1989. PCR technology: Principles and amplifications for DNA amplification . Stockton Press, New York. 4. Innis, M.A., D.H. Gelfand, J.J. Sninsky, and T.J. White. 1990. PCR...
  7. ...-CoV-2. In this setting, sensitivity determines how well the detection tests can capture the diversity of all SARS-CoV-2 variants. Lack of sensitivity leads to an increase in false-negative qRT-PCR results, because two or more mismatches can result in increases in CT values and degradation in accuracy...
  8. ...(Supplemental Table 4) were first generated as dsRNAs from PCR products (received from the NYU RNAi Core Facility). Amplification by PCR was followed by in vitro transcription reactions of the cDNA PCR products into dsRNA using the Ambion MEGAscript T7, T3, and SP6 kits (Life Technologies). The secondary screen...
  9. ...with a simulated annealing algorithm to minimize off-target amplification and maximize efficiency at capturing all possible breakpoints within the target regions. To confirm correct amplification and obtain breakpoints, PCR amplicons are combined without barcoding and simultaneously long-read sequenced using...
  10. ...cell line, we detected a GAPF-positive region at the centromeric breakpoint of a complex copy-number gain in 8q24.21 that contains the MYC oncogene (Fig. 3A). We next confirmed that the GAPF signal represented a cancer-specific palindrome. A regional PCR-based enrichment analysis following the S1...
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