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Micro ch10 Biotech Test

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1.
Biochemical Products of Recombinant DNA Technology
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2.
Restriction endonucleases
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3.
Priming
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4.
When was the last time you cloned something? What was it? Why was it a clone?
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Antisense DNA
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Recombinant DNA technology
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DNA technology as genetic medicine
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Sticky ends
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DNA fingerprinting
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Southern blot method
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Vectors
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Reverse transcriptase
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Technical aspects of recombinant DNA and gene cloning
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Primers
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Steps in PCR cycle
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Sanger method
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Genetically Modified Organisms
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Denaturation
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Polymerase chain reaction
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Characteristics of cloning vectors
A.
A unique picture of a genome
B.
Human growth hormone, Insulin, Clotting factor VIII
C.
receiver of propagated gene from another organism; usually a plasmid or virus; it will insert the DNA into the cloning host.
D.
finding target gene on donor chromosome and isolating it. DNA removed from cells, separated into fragments; fragments inserted into vector and cloned; cloned frags undergo southern blotting and are probed to ID desired sequences (long process). OR gene c
E.
technique that separates fragments of DNA using electrophoresis and identifies them by hybridization
F.
the short tails of severed DNA
G.
DNAs formed in first cycle become amplicons upon denaturization; heating target DNA to 94 degrees C to separate it into two strands; then system is cooled to between 50 and 65 depending on nucleotide sequence
H.
must be capable of carrying a significant piece of donor DNA; must be readily accepted by the cloning host, must have a promoter in the front of the cloned gene.
I.
Working with my lab unknown;created a streak plate of the organism from a broth sample. It is a clone because the colonies on the streak plate are genetically identical to the parent cells that I obtained from the broth sample.
J.
it is through cyclic repetition of these steps that DNA becomes amplified; denaturation, priming, extension
K.
Used in labs to cleave the strand at desired sites
L.
Targeting mRNA; when binds to its particular mRNA the double-stranded RNA is inaccessible to the ribosome, resulting in loss of translation of that mRNA; the reading of that mRNA transcript on ribosomes will be blocked and the gene product will not be syn
M.
synthetic oligonucleotides; landmarks for where DNA amplification should begin
N.
based on synthesis and analysis of complementary strand of DNA in a test tube.
O.
treatment prevents transcription or translation of a gene that is unwanted.
P.
to deliberately remove genetic material from one organism and combine it with that of a different organism.
Q.
Xerox machine for DNA; increases amt DNA in sample w/out cultures or carrying out complex purification techniques; “plucks” a DNA “needle out of a haystack;” same events as DNA synthesis (unzipping, addition of primers, action of DNA polymerase)
R.
enzyme; converts RNA into DNA
S.
primers added in a concentration that favors binding to the complementary strand of test DNA; reaction prepares the two DNA strands now called amplicons for synthesis.
T.
Recombinant organisms produced through introduction of foreign genes are called transgenic or genetically modified organisms (GMOs).
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21.
Genetics is considered what kind of science?
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Genetic engineering is what kind of science?
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23.
pieces of DNA produced by restriction endonucleases
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sequences of DNA that are identical when read from the 5’ to 3’ direction of one strand and the 5’ to 3’ direction on the other strand. (ex. eye, racecar)
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normal gene is cloned in vectors (retroviruses or adenoviruses). Tissues from patient are incubated w/ these viruses to transfect them with the normal gene. The transfected cells are then reintroduced into the patient’s body by transfusion.
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genetic clones; have same parental DNA
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uniting of two different nucleic acids at their complementary regions; different combos possible (single DNA with other single RNA or DNA, RNA with other RNA; allows for specially formulated oligonucleotide tracers (gene probes)
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can be made from mRNA, tRNA, rRNA, et al. Provides valuable means of synthesizing eukaryotic genes from mRNA transcripts.
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therapy skips the intermediate step of incubation; instead, naked DNA or a virus vector is directly introduced into the patient’s tissues.
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removal of selected gene from genetic donor followed by its propagation in different host organism; Gene inserted into vector (usually plasmid/virus) that will insert the DNA into cloning host

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