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DIR RD 4C-2
DIR RD 4C-2

... 12. List two examples of things proteins help determine about you. ____________________________________________________________________ ____________________________________________________________________ ...
Practice Multiple Choice- Set 1 - mvhs
Practice Multiple Choice- Set 1 - mvhs

... 13. Translation is the second step of protein synthesis. How does the translation of RNA into protein begin? a) A G cap is added to the RNA b) The promoter sequence is recognized c) A release factor binds to the RNA d) Transcription Factors bind to the RNA e) The start codon is recognized by the rib ...
Genetic engineering 2 - web.biosci.utexas.edu
Genetic engineering 2 - web.biosci.utexas.edu

... charge, some cells endocytose the complex. 3. Combine (1) and (2) ...
Cloning
Cloning

... The principle of library construction is basically quite simple.  Cut a DNA vector at a unique restriction site and ligate into it the DNA that you want to make a library out of.  If you want a library of human genomic DNA, you use fragmented human DNA.  The ligation mix is not yet considered the ...
Chapter 13 - Auburn CUSD 10
Chapter 13 - Auburn CUSD 10

... then cooled to allow replication to take place. This is done multiple times to make thousands or millions of copies of a gene. (Each time you double the number.) ...
Lect2 Genetics
Lect2 Genetics

... DNA polymerase can only extend 5’ to 3’. Leading strand is generated normally, lagging strand goes opposite way so is done in ‘Okazaki’ ...
PowerPoint® slides
PowerPoint® slides

... LIMITED TO THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE. University will not be liable for any costs, damages, fees or other liability, nor for any direct, indirect, special, incidental or consequential damages (including lost profits) with respect to any claims by ...
Genetics – Human Genetic Disorders and Genetic Engineering
Genetics – Human Genetic Disorders and Genetic Engineering

... from many cells into manageable pieces. 2. There will be a collection of copies of fragment 1, which is a different size than fragment 2, and so on. 3. The pieces can be ordered according to size using gel electrophoresis (moving the fragments in an electric field through a gel matrix). Larger piece ...
Slide 1 - New Century Academy
Slide 1 - New Century Academy

... -6 billion base pairs -Genome will fill 1,200 AP bio books -Replicated in just a few hours -Errors occur in 1/10 billion base pairs -Most of Replication is known about prokaryotic cells – Eukaryotic is similar to ...
Reporting Category 2
Reporting Category 2

... •Uses complementary nucleotides just like replication •Except that A pairs with U instead of T ...
Gene Cloning 2
Gene Cloning 2

... • When the source of DNA is small or impure, the polymerase chain reaction (PCR) is quicker and more selective. (limitation of PCR -- produces short DNA segments within a gene and not entire genes.) • This technique can quickly amplify any piece of DNA without using cells. • Devised in 1985, PCR has ...
E coli
E coli

... • Bacterial chromosome is a large (4 Mb in E coli) circular molecule • Bacterial cells may also contain small circular chromosomes called plasmids (4kb - 100kb; 1 - 1000 copies) that code for optional functions such as antibiotic resistance • Will look at circular DNA in this lecture • The bacterial ...
10 Worksheet 9 Handout for powerpoint Applying our Knowledg
10 Worksheet 9 Handout for powerpoint Applying our Knowledg

... screening techniques in an effort to reduce the frequency of children born with genetic abnormalities.” c) “As long as there are strict guidelines controlling gene therapy, society will not have to be concerned about abuses of this technology.” d) “Private biotech companies that have invested millio ...
recombinant dna and polymerase chain reactions
recombinant dna and polymerase chain reactions

... It is necessary to isolate the host bacteria that contain the gene that has been spliced as only want the recombinant DNA By having a gene on the same plasmid that gives resistance to an antibiotic, the other bacteria can be removed by culturing the bacteria in a medium that contains the antibiotic. ...
Jatropha genotyping In Gh Pu QR In Gh Pu QR 13 primer pairs
Jatropha genotyping In Gh Pu QR In Gh Pu QR 13 primer pairs

PCR - share1
PCR - share1

... (E. coli is most common host, but yeasts or other cell types work.) ...
Cell Cycle SG
Cell Cycle SG

... Major Event(s) ...
centromere
centromere

... • Telomeres and centromeres contain special DNA sequences and associated proteins • Telomeres are replicated differently from the rest of the genome - see figure 26.37 in Lehninger • Different regions of the chromosome can be stained with dyes (e.g. Giemsa) giving a characteristic banding pattern ...
DNA Replication Practice Worksheet
DNA Replication Practice Worksheet

... The double helix of DNA unwinds and each side serves as a pattern to make a new molecule. Image courtesy U.S. Department of Energy Human Genome Program DNA Replication DNA carries the information for making all of the cell's proteins. These proteins implement all of the functions of a living organis ...
houston community college
houston community college

... Understand the different types of recognition sequences for restriction enzymes (not the actual sequences). Why has the Polymerase Chain Reaction revolutionized genetics? What does it do? In gel electrophoresis, which DNA fragment (in terms of size) would migrate further from the sample well? Unders ...
DNA: The Molecule of Heredity
DNA: The Molecule of Heredity

... DNA is called the double helix because it is a two sided, twisted ladder. ...
DNA Test Review What are the four nucleotides in DNA? Which
DNA Test Review What are the four nucleotides in DNA? Which

... 12. Why is tRNA important in translation? 13. What is the difference between DNA and RNA? 14. How many amino acids does this DNA sequence represent: TAAAGGCCC? 15. How can only 20 amino acids make thousands of proteins? 16. What is the ratio of A:T and C:G? 17. Why is DNA replication called semicons ...
1 - web.biosci.utexas.edu
1 - web.biosci.utexas.edu

... c. oxidation of guanine to 8-oxo-guanine d. b and c e. all of the above 8. Which of the following is not true regarding DNA photolyases a. repair thymidine-thymidine dimers by a redox-related mechanism b. have FAD as an electron donor and chromophore c. use mainly UV-A and blue light for repair d. c ...
Systematic Implications of DNA variation in subfamily Opuntioideae
Systematic Implications of DNA variation in subfamily Opuntioideae

Recombinant DNA and Cloning
Recombinant DNA and Cloning

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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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