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Ch. 20 Bio Notes Quiz
make use of crops such as corn and soybeans to replace fossil fuels
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coal
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biotechnology
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biofuels
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cloning
small circular DNA molecule obtained from a bacterium; serves as a cloning vector
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pcr
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dna ligase
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cdna
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plasmid
proteins that are important tools for gene cloning and manipulation*
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restriction enzymes
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pcr
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dna ligase
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primers
one method of rapidly analyzing and compairing DNA samples*
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genetic engineering
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agarose gel electrophoresis
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cloning and manipulation
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PCR and gel electrophoresis
the manipulation of organisms or heir genetic components to make useful products
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recombinant dna
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genetic engineering
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cloning
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biotechnology
most methods for cloning DNA in the laboratory share general features, like the use of ______
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bacteria and their plasmids
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antibiotic resistance genes
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recombinant plasmid
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DNA microarray assays
process where a bacterium takes up a plasmid from the surrounding solution
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restriction enzymes
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pcr
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transformation
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cloning
x-gal is hydrolyzed by the lacZ gene product, B-galactosidase, to yeild a _____ product.
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bases of sticky ends
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blue pigmented
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transformation
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genetic profile
plasmids used to clone genes
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dna ligase
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thermostable dna polymerase
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cdna
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cloning vector
detects DNA differences that affect restriction sites*
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agricultural productivity
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restriction fragment length polymorphisms
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cloning and manipulation
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restriction fragment analysis
within a living organism (opposite of in vitro)
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in situ hybridization
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in vivo
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transformation
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in vitro
to work directly with specific genes, scientists must prepare large quantities of gene-sized fragments of DNA in identical copies
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intruding DNA
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DNA cloning
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foreign DNA
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cloning
one way to _____ is to disable the gene and observe the consequences.
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PCR and gel electrophoresis
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high spealized cells
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determine gene function
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genetic engineering
a cloning vector is a DNA molecule that can carry _____ into a host cell and replicate within the host cell
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an origin of replication
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a restriction nuclease cut site
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recombinant Dna
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foreign DNA
____ can hybridize (form base pairs) via hydrogen bonding with complementary bases ( A-T & G-C)
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blue pigmented
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buffered solution
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bases of sticky ends
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short tandem repeats
useful for making many copies of a particular gene and for producing gene products (protein or RNA)
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cloned genes
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blue pigmented
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sticky ends
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endonucleases
variations in DNA sequence
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short tandem repeats
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polymorphisms
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mutations
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anode
allow for maintenance of the plasmid in bacterial host, usuallt the bacterium (E. coli-Escherichia coli)
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tail fiber genes
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restriction enzymes
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antibiotic resistance genes
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water in its cytoplasm
enzyme that forms covalent bonds between restriction fragments
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Primers
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Cdna
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Restriction enzymes
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DNA ligase
in gene cloning, DNA from an organism of interest is inserted into a plasmid, usually using an _______
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genetic profile
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DNA microarray assays
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electrical current
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in vitro reaction
restrictio enzymes were discovered in bacteria, where they function to protect bacteria against intruding DNA from other organisms, such as bacteriophages
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intruding DNA
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sticky ends
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denaturation
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recombinant DNA
The sticky end of the DNA restriction fragment -TGCA will pair with a DNA fragment with the sticky end ____.
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plasmid
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-ACGT
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X-gal
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lacZ gene
outside a living organism (as in a test tube)
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pcr
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live
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in vivo
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in vitro
The ___ the DNA molecule, the farther it moves.
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same length
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longer
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shorter
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the same size
2nd step in a PCR; lower temperature incubation allows single-stranded complementary template DNAs and DNA primers to anneal*
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extension
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denaturation
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annealing
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transformation
(STRs); varitations in the number of repeats of specific DNA sequences in a genome
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short tandem repeats
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restriction fragment length polymorphisms
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sticky ends
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cloning
reproduction of the transformed bacterial cells results in _____ of the recombinant plasmid
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cloning
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pcr
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transformation
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genetic engineering
in PCR; heat-tolerant DNA strands
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Dna ligase
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Rna primers
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Thermostable DNA polymerase
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Template dna
colonies of bacteria transformed with nonrecombinant plasmids containing intact lacZ genes will be ___ in color.
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blue
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white
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green
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red
of genes involves the use of recombinant DNA technologies
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determine gene function
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restriction fragment analysis
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cloning and manipulation
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agarose gel electrophoresis
in order to insert a human gene into a plasmid, both must be cut by the ________; doing so will result in the formation of complementary sticky ends
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antibiotic resistance genes
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same restriction enzyme
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electrical current
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buffered solution
bond
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annealing
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extension
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anneal
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cloning
restriction enzymes are ____ that ut (hydrolyze) DNA moelcules at specific sequences, usually palindromic, called restriction sites
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endonucleases
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template dna
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dna ligase
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probes
compound used to identify colonies produed by bacteria transformed with recombinant, lacZ disrupted plasmids.
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Lacz
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Annealing
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X-gal
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Cdna
multiple cloning site; has restriction enzyme cut sites
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TRANSFORMATION
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PLASMID
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MCS
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PCR
DNA microarray assays ____ of gene expression in different tissues, at different times, or under different conditions*
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transgenic animals
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buffered solution
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compare patterns
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mutants phenotype
automation has allowed scientists to measure expression of thousands of genes at 1 time using _____*
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DNA microarray assays
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in vitro reaction
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antibiotic resistance genes
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restriction enzymes
can be used to identify where or when a gene is transcribed in an organism
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probes
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pcr
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restriction enzymes
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primers
using ______, mutations are introduced into a cloned gene, thereby altering or destroying its function
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in situ hybridization
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in vitro mutagenesis
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rna interference
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genetic engineering
in _____ , nucleotide sequences from 2 different sources (often consisting of sequences from 2+ different species)are combined in vitro into the same DNA molecule.
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biotechnology
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genetic Engineering
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recombinant DNA
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plasmid
can be used to modify the metabolism of microorganisms
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genetic engineering
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cloning
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recombinant dna
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biotechnology
in PCR; contains the taret DNA sequence to be amplified*
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Ribosomal Rna
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Template DNA
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Primers
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Dna
in PCR; provides a suitable, pH stabilized chemical environment required for optimum activity and stability of the DNA polymerase*
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buffered solution
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strong acid
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temperature greater than 100 degrees centigrade
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buffered
collection of recombinant vector clones produced by cloning DNA fragments from an entire genome*
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sticky ends
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pcr
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genomic library
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recombinant plasmid
positively charged
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anode
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negative pole
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north pole
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cathode
complementary DNA; made by cloning DNA made *
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template dna
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recombinant dna
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cDNA
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plasmid
gene therapy is likely to be most successful with diseases caused by_____
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chromosomal abnormalities
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genetic imprinting
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incomplete dominance
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single gene defects
colonies of bacteria transformed with recombinant plasmids with disrupted lacZ genes will be ___, since they do not produce functional B-galactosidase
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red
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white
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blue
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gray
negative charged
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casting tray
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cathode
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voltometer
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anode
3rd step of a PCR; DNA polymerase catalyzes synthesis of new strands of DNA complementary to the DNA template*
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extension
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denaturation
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annealing
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cloning
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