نتایج جستجو برای: restriction endonuclase enzyme
تعداد نتایج: 308200 فیلتر نتایج به سال:
several reports have indicated that infection with non-tuberculosis mycobacteria (ntm) is increasing worldwide.therefore,monitoring species causing micobacterial infection in any region is of great importance. this study was going to detect, differentiate, and identify pathogenic mycobacteria in primary clinical samples. eighty samples collected from tuberculosis suspected patients in isfahan/i...
Background and Objective: Uricase (EC 1.7.3.3) is an enzyme which catalyses uric acid to H2O2 and alantoin and is utilized in the treatment of hyperuricemia or gout. The aim of this study was cloning of Aspergillus flavus uricase synthetic gene into pET-28(a) and its recombinant expression in E. coli Materials and Methods: The coding sequence of uricase retrieved from gene bank and once opti...
We have Investigated the use of dU excision by uracil N-glycosylase (UDG) to create cohesive ends on PCR fragments "mimicking" those generated by restriction enzymes. The feasibility of this approach for directional and nondirectional cloning using cohesive ends mimicking Sacl or Pstl ends is demonstrated by the subcloning of a 383 to 388-bp fragment of bovine basic flbroblast growth factor int...
We have investigated the use of dU excision by uracil N-glycosylase (UDG) to create cohesive ends on PCR fragments "mimicking" those generated by restriction enzymes. The feasibility of this approach for directional and nondirectional cloning using cohesive ends mimicking SacI or PstI ends is demonstrated by the subcloning of a 383 to 388-bp fragment of bovine basic fibroblast growth factor int...
Background and purpose: The purpose of this study was to design a recombinant vector pEFGP- N1 containing the full length of HIV-1Vpr gene. To the best of our knowledge, the cloning of Vpr gene in pEGFP_N1 is not previously done. Materials and methods: As a source of Vpr gene the pUC19-Vpr recombinant vector was confirmed by digestion with restriction enzymes BglII and NotI in order to separ...
Requirement of divalent cations for DNA cleavage is a general feature of type II restriction enzymes with the exception of few members of this group. A new type II restriction endonuclease has been partially purified from Lactococcus lactis KLDS4. The enzyme was denoted as LlaKI and showed to recognize and cleave the same site as FokI. The enzyme displayed a denatured molecular weight of 50 kDa...
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