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Alteration by site-directed mutagenesis of the
Alteration by site-directed mutagenesis of the

... RecB mutagenesis RecB gene subcloning. The plasmid pDJ02 (11), containing a 13.5 kilo-base pair (kb) Smal-BamHI fragment encoding the recBCD genes, was digested with Xhol to produce a 3166 basepair (bp) fragment (nucleotides # 7,947—11,112 according to the numbering in (16,17)) containing part of th ...
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... and Indian childhood hepatic cirrhosis. Studies of the genomic organization of the human C3 gene led to the identification of a single change (C to G) between C3 S and C3 F at nucleotide 364 in exon 3 . This leads, at the translation level, to the substitution of an arginine residue (positively char ...
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The influence of low-molecular-weight heparin (LMWH

... in the embryonic tissue, that is, the set of chromosomes of the placenta is not always identical to the set of chromosomes of the fetus. Following chorionic villus sampling (CVS), this leads to fetoplacental discrepancies in approximately 1 to 2% of cases. These mosaics limited to the placenta can a ...
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Molecular cloning



Molecular cloning is a set of experimental methods in molecular biology that are used to assemble recombinant DNA molecules and to direct their replication within host organisms. The use of the word cloning refers to the fact that the method involves the replication of one molecule to produce a population of cells with identical DNA molecules. Molecular cloning generally uses DNA sequences from two different organisms: the species that is the source of the DNA to be cloned, and the species that will serve as the living host for replication of the recombinant DNA. Molecular cloning methods are central to many contemporary areas of modern biology and medicine.In a conventional molecular cloning experiment, the DNA to be cloned is obtained from an organism of interest, then treated with enzymes in the test tube to generate smaller DNA fragments. Subsequently, these fragments are then combined with vector DNA to generate recombinant DNA molecules. The recombinant DNA is then introduced into a host organism (typically an easy-to-grow, benign, laboratory strain of E. coli bacteria). This will generate a population of organisms in which recombinant DNA molecules are replicated along with the host DNA. Because they contain foreign DNA fragments, these are transgenic or genetically modified microorganisms (GMO). This process takes advantage of the fact that a single bacterial cell can be induced to take up and replicate a single recombinant DNA molecule. This single cell can then be expanded exponentially to generate a large amount of bacteria, each of which contain copies of the original recombinant molecule. Thus, both the resulting bacterial population, and the recombinant DNA molecule, are commonly referred to as ""clones"". Strictly speaking, recombinant DNA refers to DNA molecules, while molecular cloning refers to the experimental methods used to assemble them.
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