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2015 Test 3 study guide Bio 105
2015 Test 3 study guide Bio 105

... • Tools for DNA manipulation- restriction enzymes, reverse transcriptase, gel electrophoresis, PCR, gene machines, micropipettes, computer control robotics, genomic libraries, and genomic data bases 6.15 Genetically modification • What is a genetically modified organism • Examples of GMO and their u ...
IB Biology 11 SL (H) - Anoka
IB Biology 11 SL (H) - Anoka

... State that a human female can be homozygous or heterozygous with respect to sex-linked genes Explain that female carriers are heterozygous for X-linked recessive alleles Predict the genotypic and phenotypic ratios of offspring of monohybrid crosses involving any of the above patterns of inheritance ...
Bacterial plasmids
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Ch.6.2Review - Cobb Learning
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... ribosome. _____ 19. Transfer RNA molecules deliver amino acids to the ribosome. _____ 20. Transfer RNA molecules pick up amino acids from the cytoplasm. ...
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... •DNA has a negative charge on its particles. • Molecules sort based on: •Charge - The greater the charge the more pull. •Size – Bigger pieces are slower, smaller are faster. •Shape - Coiled is slower straight is faster. •The negatively charged particles move toward the positive electrode while the p ...
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... an activity that affected selective markers in many strains. The filtrates also contained a temperate phage. Because of how little we knew about phage or temperate phage at the time (1950-1951), this finding wasn't all that helpful. In a not quite straight path of research and analysis, we finally s ...
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A one-step cloning method for the construction of somatic cell gene

... and then numerous cloning steps. It is an extremely time-consuming process and limited by the available unique restriction enzyme sites in the vector and in the two amplified homologous fragments. Phage-based Escherichia coli homologous recombination systems [7-9] have been developed that now make i ...
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... Chain-termination strand synthesis by a DNA polymerase is illustrated for the G reaction in the figure at left below. To prevent all chains from terminating at the first G position, ddGTP is added at ~1/100th the amount of dGTP. To achieve termination at each type of base, four separate reactions ar ...
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Bacterial Genetic

... • E.coli would prefer to use glucose as its fuel • If glucose is scarce, cyclic AMP is abundant and serves as an allosteric activator to a regulatory protein called CAP  stimulates RNA pol and transcription of enzymes that metabolize lactose • If glucose is availabe, cyclic AMP (cAMP) is absent  C ...
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... and high-throughput discovery of small RNAs can provide a comprehensive view of their function. Pamela Green (University of Delaware, Newark, USA) described how she and her collaborators have developed a sequencing method to identify and quantify these RNA molecules by modifying the massively parall ...
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Understanding Domestication and Breeding by

... Generally speaking, the path of sequencing to practice is like this:  Genome scale-At this stage we focus on the quality of the genomes, from draft to high quality to complete;  Population scale-we mine the variations in the populations, elucidate their features;  Panel scale-we prepare enough d ...
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... The following is a list of the main themes covered in this chapter and some study objectives. As you study, focus on these areas. Understand how the information you study fits into these themes and how these themes relate to each other. Be sure you master each objective before moving on. 1. Various ...
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... p = plasmid, B = Bolivar, R = Rodriguez, the cocreators of this plasmid Much used in genetic engineering as a vector ...
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... growth (called crown gall), bacterium contain large Ti plasmid where T DNA moves from bacterium and integrates into plant cell chromosomes, 25 bp repeats and vir genes are essential ...
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... One gene of an insertion sequence codes for transposase, which catalyzes the transposon’s movement. The inverted repeats, about 20 to 40 nucleotide pairs long, are backward, upside-down versions of each other. In transposition, transposase molecules bind to the inverted repeats & catalyze the cuttin ...
Powerpoint Presentation: Gene Transfer
Powerpoint Presentation: Gene Transfer

... mRNA from cells making the desired protein is extracted  Reverse transcriptase used to make cDNA  cDNA used to make gene probes  Gene located on a chromosome  Gene sequenced  Gene bracketed by sequences cut by a restriction enzyme  Gene cut out using restriction enzyme ...
Ch. 18 – Microbial Models of DNA
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Ch. 18 – Microbial Models of DNA
Ch. 18 – Microbial Models of DNA

... start lytic cycle • “latent” phase ...
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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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