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  2. Cloning vector - Wikipedia

    en.wikipedia.org/wiki/Cloning_vector

    A cloning vector is a small piece of DNA that can be stably maintained in an organism, and into which a foreign DNA fragment can be inserted for cloning purposes. [1] The cloning vector may be DNA taken from a virus , the cell of a higher organism, or it may be the plasmid of a bacterium.

  3. Cosmid - Wikipedia

    en.wikipedia.org/wiki/Cosmid

    A cosmid is a type of hybrid plasmid that contains a Lambda phage cos sequence. [1] Often used as cloning vectors in genetic engineering, cosmids can be used to build genomic libraries. They were first described by Collins and Hohn in 1978. [2] Cosmids can contain 37 to 52 (normally 45) kb of DNA

  4. Restriction modification system - Wikipedia

    en.wikipedia.org/wiki/Restriction_modification...

    The RM system was first discovered by Salvatore Luria and Mary Human in 1952 and 1953. [1] [2] They found that a bacteriophage growing within an infected bacterium could be modified, so that upon their release and re-infection of a related bacterium the bacteriophage's growth is restricted (inhibited; also described by Luria in his autobiography on pages 45 and 99 in 1984). [3]

  5. Lambda phage - Wikipedia

    en.wikipedia.org/wiki/Lambda_phage

    Bacteriophage Lambda Structure at Atomic Resolution [1] Enterobacteria phage λ (lambda phage, coliphage λ, officially Escherichia virus Lambda) is a bacterial virus, or bacteriophage, that infects the bacterial species Escherichia coli (E. coli). It was discovered by Esther Lederberg in 1950. [2]

  6. Mobile genetic elements - Wikipedia

    en.wikipedia.org/wiki/Mobile_genetic_elements

    Before site specific recombination can occur, the oligonucleotide ends must be filled. The ligation of these ends generates a replication fork at each end of the transposable element. The single strand displacement causes synthesis from the un-ligated 3' hydroxyl group to form long single stranded sections adjacent to the 5' end.

  7. Site-specific recombination - Wikipedia

    en.wikipedia.org/wiki/Site-specific_recombination

    Site-specific recombination systems are highly specific, fast, and efficient, even when faced with complex eukaryotic genomes. [4] They are employed naturally in a variety of cellular processes, including bacterial genome replication , differentiation and pathogenesis , and movement of mobile genetic elements . [ 5 ]

  8. Phage typing - Wikipedia

    en.wikipedia.org/wiki/Phage_typing

    Phage typing is a phenotypic method that uses bacteriophages ("phages" for short) for detecting and identifying single strains of bacteria. [1] Phages are viruses that infect bacteria and may lead to bacterial cell lysis. [2] The bacterial strain is assigned a type based on its lysis pattern. [3]

  9. Phage display - Wikipedia

    en.wikipedia.org/wiki/Phage_display

    Phage display cycle. 1) fusion proteins for a viral coat protein + the gene to be evolved (typically an antibody fragment) are expressed in bacteriophage. 2) the library of phage are washed over an immobilised target. 3) the remaining high-affinity binders are used to infect bacteria. 4) the genes encoding the high-affinity binders are isolated.

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