Restriction enzyme scissor cut

How the BfiI restriction enzyme uses one active site to cut two DNA strands.

Unlike other restriction enzymes, BfiI functions without metal ions. It recognizes an asymmetric DNA sequence, 5'-ACTGGG-3', and cuts top and bottom strands at fixed positions downstream of this sequence. Many restriction enzymes are dimers of identical subunits, with one active site for each DNA strand. Others, like FokI, dimerize transiently during catalysis. BfiI is also a dimer but it has o...

Restriction Enzyme Recognition Sequence

A critical and difficult part of characterizing restriction enzymes and methylases is the identification of recognition sequences. To simplify this process, we have developed a plasmid transformation method along with a computer program named RM search that determines the exact recognition sequences for given restriction and modifica-

'Scissor deformity' of the toes.

Haptoglobin gene subtyping by restriction enzyme analysis.

cell membrane (PS exposure detected by Annexin V binding) events. This is the first time that fetal NRBCs in the maternal circulation have been examined for PS exposure. Our analysis also differs from a recent report made by Kolialexi et al. (13), who reported a high percentage of Annexin V-positive fetal cells in the maternal circulation, which were proposed to be of an apoptotic nature. A maj...

DNA cloning without restriction enzyme and ligase.

One common problem in using the traditional DNA cloning procedure is that suitable natural restriction sites are often unavailable for a given task. Creating new restriction sites is often time consuming. Here, I describe a simple technique of producing "customized cohesive ends" by a combination of PCR primer design and lambda exonuclease digestion. These complementary cohesive ends can form h...