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1 ction enzyme and its methylation-insensitive isoschizomer.
2 ergence displayed by two homing endonuclease isoschizomers.
3 mation about recognition and cleavage sites, isoschizomers, commercial availability, crystal and sequ
4 references, recognition and cleavage sites, isoschizomers, commercial availability, crystal and sequ
5 references, recognition and cleavage sites, isoschizomers, commercial availability, methylation sens
6 references, recognition and cleavage sites, isoschizomers, commercial availability, methylation sens
7 -binding proteins, and demonstrates that the isoschizomers display strikingly different protein/DNA c
8 At the same time, MlyI endonuclease, a PleI isoschizomer, does not exhibit any DNA nicking/cleavage
9 n enzymes with new recognition sites and two isoschizomers (EcoBI and Eco377I) were identified in a c
10 or almost identical protein sequences, while isoschizomers from distant sites demonstrate considerabl
12 cleavage preference of I-TevI to that of the isoschizomer I-BmoI which targets a different cleavage s
13 ht of 22 base-pairs, and the structure of an isoschizomer, I-MsoI, bound to a nearly identical DNA ta
15 the methylation-sensitive restriction enzyme isoschizomers MspI and HpaII, and subjected to Southern
16 mation about recognition and cleavage sites, isoschizomers, neoschizomers, commercial availability, m
17 mation about recognition and cleavage sites, isoschizomers, neoschizomers, commercial availability, m
21 e cloning vector using BspQI, an inexpensive isoschizomer of SapI, and increased the efficiency of ge
22 In addition to the previously recognized isoschizomers of AvaI and AvaII, PCC 7120 was found to p
23 ' revealed that they produce seven different isoschizomers of the prototypes: EcoAI, EcoBI, EcoKI, Ec
26 We present here the structure of a BamHI isoschizomer, OkrAI, bound to the same DNA sequence (TAT
27 r no sequence homology with the exception of isoschizomers, or enzymes that recognize and cleave the
31 re based on the use of methylation-sensitive isoschizomer restriction enzyme pairs and/or sodium bisu
32 fied, 11 are conserved between EcoRI and the isoschizomer RsrI (which shares 50% identity), a further
33 essing a 5' overhang integrated into a KpnI (isoschizomer) site possessing a 3' overhang, most likely
34 ensitive and -insensitive restriction enzyme isoschizomers, Southern blots probed with chloroplast an
38 spI, we increase the representation by these isoschizomers to more than 1.32 million loci in the huma
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