Searching journal content for articles similar to Wilkinson et al. 4 (6): 363.

Displaying results 1-10 of 4740
For checked items
  1. ...was recovered, quantified by qPCR, and sequenced. (B) A 20-bp-long p53BS (low and high affinity) was placed at different positions 0, 5, 41, 46, 66, 71, and 81 bp away from the dyad. The superhelix location (SHL) is designated for each nucleosome sequence. (C) Within the nucleosome, three different positions...
  2. ...Determining the impact of uncharacterized inversions in the human by droplet digital PCR Marta Puig1, Jon Lerga-Jaso1, Carla Giner-Delgado1, Sarai Pacheco1, David Izquierdo1, Alejandra Delprat1, Magdalena Gayà-Vidal2, Jack F. Regan3, George Karlin-Neumann3 and Mario Cáceres1,4 1Institut de...
  3. ...Measurement of the abundance of nuclear and cytoplasmic mRNA was performed as described previously (Wang et al. 2006). In short, cells were lysed, nuclei were pelleted by centrifugation, and the supernatant was collected as cytoplasmic fraction. Next, RT-PCR was performed on both fractions, followed by qPCR quantification...
  4. ..., solubilized chromatin was incubated with pAG Dynabeads, preloaded with 3 ug of antibody overnight, then sequentially processed through A-tailing, first adapter ligation, Phi29 fill-in, lambda exonuclease digestion, cross-link reversal, second adapter ligation, and PCR for final high-throughput sequencing...
  5. ...conducted as described previously (Tzelepis et al. 2016).Additional information on cell culture, Native ChIP, crosslinked ChIP, DNA methylation analysis, FAIRE, Western blotting, immunofluorescence analysis, cDNA synthesis, qPCR, RNA-seq analysis, ChIP-seq analysis, knockdown analysis, peptide binding assay...
  6. ...-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...
  7. ...-bp fragments of the cell cycle sensors, GFP-CDT1 and GFP-GMNN, containing the coding region of the GFP were PCR-amplified from GFP-CDT1 and GFP-GMNN synthetized gBlocks (Integrated DNA Technologies [IDT]) using the corresponding primers (Supplemental Table S7). The primers contain EcoRI restriction...
  8. ...of mtDNA as a biomarker highlights the need for a more high-throughput method of mtDNA quantification. The current standard employed in the measurement of mtDNA copy number is quantitative PCR (qPCR). Measurements by qPCR require the use of a reference gene and are often displayed as a ratio...
  9. ...pooled library was a gift from Feng Zhang (Addgene #1000000048) (Sanjana et al. 2014). The oligo pool for the focused library was purchased from CustomArray, Inc. The single-stranded oligos were amplified to double-stranded DNA by PCR and assembled to a lentiviral sgRNA plasmid using NEBuilder HiFi DNA...
  10. ...indicate a homozygous variant or a pathogenic repeat expansion. Subjects with a single PCR fragment were selected for RP-PCR, and PCR products were analyzed with an ABI 3730 DNA Analyzer and GeneMapper software. If the RP-PCR revealed a characteristic stutter pattern, these individuals were screened using...
For checked items

Preprint Server