A composition for sequencing DNA is provided and comprises a nuclease and a nuclease-resistant sequencing primer.
Nuclease cleaved heteroduplexes can be easily distinguished from nuclease uncleaved heteroduplexes by differential labeling.
This invention provides the use of Ache as nuclease.
In many cases, the in vitro translation reaction comprises at least one nuclease, which may be a ribonuclease, a deoxyribonuclease, or a nonspecific nuclease.
Enzymatically active variants of nuclease from Serratia marcescens (nuclease [S.m.]) are disclosed, which do not dissociate into subunits.
An extracellular ribonuclease of a Serratia Mercenses bacterium can be used in the form of said agents.
The translation product, a nuclease referred to as "Nucyep" is biologically active.
The nuclease may be employed to remove nucleic acids from a biological material.
The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., ribonuclease) substrates, and probes and compositions useful in detection assays.
A thermostable enzyme having polymerase activity and substantially no nuclease activity is provided.
Surprisingly, nuclease activity is not decreased in the presence of chelating agents.
Methods to produce such a genetically modified pig are herein provided.In particular, the pig and cells are generated using zinc finger nuclease-mediated or Transcription activator-like effector nuclease-mediated technologies.
The nuclease part is responsible for precise cleavage of the DNA.
The cleavage structure is cleaved with a 3' nuclease and a detectable signal is produced.
Nuclease: converts nucleic acids into nucleotides and nucleosides;
Disclosed herein is a fusion protein possessing both nuclease and phosphatase activities.
These oligonucleotides demonstrate enhanced nuclease resistance, cellular uptake and biological efficacy.
A selected region of a nucleic acid is protected from attack by nuclease by complexing to the nucleic acid a nucleic acid analogue of the PNA type.
Further modification formatted siRNAs are demonstrated to be stabilized to nuclease-rich environments.
The third segment, C, is an S1 nuclease-sensitive site having CCTT repeats.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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