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The Map-based Sequence of the Rice Genome
The Map-based Sequence of the Rice Genome

LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034

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Particle bombardment
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... Electroporated pollen can supposedly germinate at 30% efficiency. However, no transgenic plant has so far been reported using this concept, even though it has been shown that pollen grains can be permeated with macromolecules such as DNA. Electroporation method is very efficient in permeating DNA in ...
MGG330 L1-2007
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Simple and straightforward construction of a mouse gene targeting

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DNA SEQUENCING DNA sequencing
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Adenine - /ad·e·nine/ - One of four bases found in the nucleotides of

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Note 8.1 - Cloning DNA

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Practice Questions 1: Genetics

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Directions for Dog Breed Genetics

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What do Genes Look Like - Effingham County Schools

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Chromomere - aqinfo.com

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DNA Replication and Cancer

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... Recombinant DNA technology 1. identify gene you want to transfer to target organism. 2. use restriction enzymes to remove the gene from the host organism. 3. use the same restriction enzymes to cut a plasmid. Now both the plasmid and the genes have the same overhangs--they can fit together like puzz ...
ppt - Barley World
ppt - Barley World

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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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