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CH 23 Part 2 Modern Genetics
CH 23 Part 2 Modern Genetics

... tracers, and then mixing the fragments in a gel. In an electric field, smaller fragments move farther along the gel, and the distribution of fragments can be recorded on a photographic film (b). Because each person’s DNA sequence is unique, each DNA fingerprint is distinctive. ...
The Avery and Hershey-Chase Experiments
The Avery and Hershey-Chase Experiments

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AIM: OBJ: DN: HW - Hicksville Public Schools / Homepage
AIM: OBJ: DN: HW - Hicksville Public Schools / Homepage

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... polymerase  at  a  promoter   region  of  DNA.   •  The  σ  subunit  is   responsible  for  promoter   recogniFon  (in  bacteria).   •  Once  iniFaFon  has  been   completed  with  the   synthesis  of  the  first  8–9   nucleoFdes,  sigma ...
DNA Fingerprinting
DNA Fingerprinting

... Northern Blot Analysis • Northern blot analysis is used for determining: – The size(s) of mRNA encoded by a gene. Northern blots have shown that different mRNA species arise from the same region of DNA, suggesting differential use of promoters and terminators, and/or alternative mRNA processing. – ...
Lab 3 minipreps, RE, gel
Lab 3 minipreps, RE, gel

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Standard 3

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Ethanol precipitation of DNA with salts

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ANSWERS TO REVIEW QUESTIONS

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Join us in downtown Chicago, July 27-29, at the
Join us in downtown Chicago, July 27-29, at the

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DNA, RNA and Protein Power Point

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PRODUK DNA REKOMBINAN

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CDOs (Creative Designer Organisms)

... demonstration of the presence of transmissible antibiotic-resistance genes in the human food chain. The resistant bacteria probably originated from antibiotic treatment of the cows. As lactococci may be found together with enterococci and staphylococci as part of the cows microflora, resistance tran ...
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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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