ライフサイエンスコーパス: type II restriction enzyme

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1 The DNA is initially fragmented with a type II restriction enzyme.

2 e cleavage of pBR322 plasmid DNA by EcoRV, a type II restriction enzyme.

3 sequence recognition by the Mg(II)-dependent type II restriction enzymes.

4 thodox enzymes, such as EcoRI and some other type II restriction enzymes.

5 shares strong similarities with a number of type II restriction enzymes.

6 ith a superfamily of nucleases that includes type II restriction enzymes.

7 or many nucleases, including MCR:A and other type II restriction enzymes.

8 etal ion to this phosphate may occur in many type II restriction enzymes.

9 turnover conditions compare favourably with type II restriction enzymes.

10 id, a task that rarely can be achieved using type-II restriction enzymes.

11 electively interfere with the action of four type IIs restriction enzymes.

12 earby B-DNA, by using a mechanism similar to type IIs restriction enzymes.

13 Type IIs restriction enzymes allow seamless assembly of

14 of a nuclease superfamily that includes the type II restriction enzymes, although their DNA cleaving

15 al domain is structurally similar to classic Type II restriction enzymes and contains the endonucleas

16 While many Type II restriction enzymes are dimers with a single DNA

17 Type II restriction enzymes are homodimeric systems that

18 Four are associated with Type II restriction enzymes (AVAI, AVAII, AVAIII and the

19 NA binding prevents endonuclease activity by type II restriction enzymes BamHI, EcoRI and SalI, and i

20 The SfiI endonuclease differs from other type II restriction enzymes by cleaving DNA concertedly

21 A second strain (CD3) possesses a type IIs restriction enzyme, Cdi I, which cleaves the se

22 While many Type II restriction enzymes consist of identical subunit

23 This technique relies upon Type IIs restriction enzyme digestion of genomic DNA and

24 In contrast to many type II restriction enzymes, dimeric proteins that cleav

25 The Type II restriction enzymes (e.g. EcoRI) gave rise to re

26 ex forming oligonucleotide (TFO) dT20 by the type IIS restriction enzyme Eco57I.

27 ion of the R2 protein appears similar to the type IIS restriction enzyme, FokI, in which specific DNA

28 ers contained a recognition site for BbvI (a type IIS restriction enzyme), followed by 11 nucleotides

29 GB2.0 relies on the use of type IIS restriction enzymes for DNA assembly and propos

30 BsoBI is a type II restriction enzyme found in Bacillus stearotherm

31 Structural and biochemical comparison with type II restriction enzymes illustrates how Vsr resemble

32 e of the endonuclease domain is analogous to type IIS restriction enzymes in that it is located on a

33 cv B73), using a variant of HICF in which a type IIS restriction enzyme is used to generate the fluo

34 e very short patch repair nuclease (Vsr) and type II restriction enzymes, is shown to encompass by fa

35 or containing a recognition site for MmeI, a type IIS restriction enzyme, is then used to release 21-

36 contrast, a modified SAGE protocol using the Type IIS restriction enzyme MmeI (generating 21-base pai

37 loys an oligonucleotide adapter containing a type IIs restriction enzyme site to facilitate the gener

38 MmeI is an unusual Type II restriction enzyme that is useful for generating

39 This method uses a type II restriction enzyme to create extendable ends at

40 ry predetermined order, using the ability of type IIS restriction enzymes to cut DNA outside of their

41 We leverage codon degeneracy and type IIs restriction enzymes to generate orthogonal liga

42 diversity of reaction mechanisms employed by Type II restriction enzymes was investigated by analysin

43 e methylation sensitivities of various known type II restriction enzymes, we identified the target ad

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