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1 eic acid labeling reactions, such as PCR and nick translation.
2  detection of DNA strand breaks with in situ nick translation.
3  quantities of complex molecules produced in nick translations.
4 clease FEN1 (Rad27), the complex carried out nick translation (1.7 nt/s).
5              Both polymerases stimulated the nick translation activity of Fen-1 on DNA- or RNA-contai
6 rted is more specific and informative than a nick translation assay for the detection of DNA strand b
7 is thaliana using the PENT (primer extension/nick translation) assay.
8           In the presence of FEN1, efficient nick translation ensues, whereby a mixture of mono- and
9                                              Nick translation experiments on isolated nuclei or cells
10 by examining DNA fragmentation using in situ nick translation histochemistry.
11 sequencing ladders by strand displacement or nick translation in the presence of trace amounts of did
12 esis and In Situ End-Labeling (ISEL)/In Situ Nick Translation (ISNT) assays reveal that the apoptotic
13         Using a DNA polymerase-mediated dUTP nick translation labeling assay, 5% or less of freshly i
14 e/helicase alone did not efficiently promote nick translation, nor did it affect nick translation wit
15        DNA polymerase I-mediated biotin-dATP nick translation (PANT) and terminal deoxynucleotidyl tr
16  using DNA polymerase I-mediated biotin-dATP nick translation (PANT) labeling.
17 ced the rate of maturation and shortened the nick-translation patch (nucleotides excised past the RNA
18 o(-) proceeded with an increased duration of nick translation prior to ligation.
19  for 24 hr with LAA and subjected to in situ nick translation showed an intense nuclear labeling of n
20                     Using a primer-extension/nick-translation technique and nondenaturing hybridizati
21  were detected in tissue sections by in situ nick translation with (35)S-radiolabeled nucleotides and
22  promote nick translation, nor did it affect nick translation with FEN1.

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