The platform also leverages a new proprietary protocol for efficient and cost-effective targeting of 10s to 100s of amplicons, allowing CE users to complete their projects in a fraction of the time at significant cost savings. ❋ Unknown (2011)
Position of the amplicons (transcription start site [TSS] and five extragenic amplicons indicated by progressive numbers) is indicated. ❋ Francesca De Santa Et Al. (2010)
(A) Diagram depicting the procedure for the MNase assay and the PCR amplicons used for the detection of Hox genes. ❋ Yongguang Tao Et Al. (2010)
(D) Agarose gel analysis of real-time RT-PCR amplicons. ❋ Claudia Filippone Et Al. (2010)
The amplicons were about 100±5 bp in size and were spaced 60±5 bp apart. ❋ Yongguang Tao Et Al. (2010)
The digested amplicons were ligated to KpnI/EcoRV co-digested ptRNA ❋ Michel V. L�vesque Et Al. (2010)
Specific primers for the corazonin ORF were designed to flank intervening sequences to readily distinguish if amplicons originated from cDNA versus contaminating genomic DNA. ❋ Yan Zhao Et Al. (2010)
The tpTAIL-PCR yielded thermal asymmetric amplicons with increasing specificity after hybridization with radioactive kDNA probe on blots of 1% agarose gel. ❋ Mariana M. Hecht Et Al. (2010)
Trim25 and Zcchc2, amplicons correspond to the Pol_II peak closest to the 5′ of the gene. doi: 10.1371/journal. pbio.1000384.g002 ❋ Francesca De Santa Et Al. (2010)
Specificity of the real-time PCR and RT-PCR results was confirmed by melting curve analysis and agarose gel electrophoresis of the amplicons for the contiguous and the non contiguous primer pairs, respectively. ❋ Claudia Filippone Et Al. (2010)
Two selected variations in the hESC lines, the deletions of the GRB10 gene in HS293 and the MLLT1 gene in HS401, were verified by designing PCR amplicons within the deleted segments. ❋ Outi Hovatta Et Al. (2010)
The position of amplicons at the TSS and upstream of the gene are indicated. doi: 10.1371/journal. pbio.1000384.g008 ❋ Francesca De Santa Et Al. (2010)
Sequencing of barcoding amplicons will be carried out by an external third party and so practical experience of conventional sequencing technology is not required. ❋ Unknown (2010)
Primers are designed to produce amplicons 100-400 bp in which the ❋ Zahoor061 (2010)
PCR amplicons were not obtained in case of 4 contigs. ❋ Nikku Raju (2010)
For each cluster the annotation of the closest neighboring UCSC known gene as well as the total number of RNA-seq transcripts, Q-PCR amplicons, and RNA repeats are shown. ❋ Francesca De Santa Et Al. (2010)
