Biology Today and Tomorrow without Physiology (MindTap Course List)
5th Edition
ISBN: 9781305117396
Author: Cecie Starr, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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- What would three possible reasons be that a PCR wouldn't work after cloning a TAQ sequence into a His-tag vector making three different constructs and verifying via SDS-PAGE that the TAQ protein is there?arrow_forwardPCR is used for cloning DNA and after about 30 cycles, the number of copies DNA will have increased about a billion times. Why is the DNA polymerase from the bacteria Thermus.aquaticus used in PCR? Because it uses primers specific to sequences in a disease causing gene or organism to diagnosis diseases, etc. O It is used to flank the gene to be copied. O It allows scientists to be able to determine the variable number of tandem repeats of minisatellites or microsatellites to determine an individual's DNA fingerprint. O It is present and needed because the enzyme is resistant to very high temperatures since the bacteria live in hot springs. Due to the walls of the he plant cell, which are thick; therefore it is used to degrade the walls for PCR to begin.arrow_forwardHow will you know if the bacterial cells were transformed during the lab? notes are attached belowarrow_forward
- Page 6 of 6 Describe the cloning vectors that would be used to clone each of the following DNA fragments: 1000 bp CDNA, 8000 bp eukaryotic gene fragment, 100,000 bp segment of a chromosome. 2leongsib 1olbrns donesas i boau ons vodb worl to slqmsxo ns sbivo1 Sa9 HEarrow_forwardMap of pUC18 is shown on the here. Describe how to select recombinant clones if a foreign DNA is inserted in to the polylinker site of pUC18 and then introduced into E. coli cells.. Hindll Sphl Sbfl Pstl BspMI Acci Hincli Sall Xbal BamHI Aval Smal Xmal Acc651 Kpnl Banll Eco53kl Sacl Apol ECORI lacz MCS LacR binding site Plac PUC18 Amp 2686 bps PMB1 oriarrow_forwardEhat primer sets could be amplify the following DNA sequence? AATACGTCGCATGGggatccttttttatgcatgarrow_forward
- Transcribe and translate the following DNA sequence (nontemplate strand): 5’-ATGGCCGGTTATTAAGCA-3’arrow_forwardWhat Are Clones? Cloning is a general term used for whole organisms and DNA sequences. Define what we mean when we say we have a clone.arrow_forwardWhich of the following best describes the process of DNA sequencing? a. DNA is separated on a gel, and the different bands are labeled with fluorescent nucleotides and scanned with a laser. b. A laser is used to fluorescently label the nucleotides present within the DNA, the DNA is run on a gel, and then the DNA is broken into fragments. c. Nucleotides are scanned with a laser and incorporated into the DNA that has been separated on a gel, and then the DNA is amplified with PCR. d. Fragments of DNA are produced in a reaction that labels them with any of four different fluorescent dyes, and the fragments then are run on a gel and scanned with a laser. e. DNA is broken down into its constituent nucleotides, and the nucleotides are then run on a gel and purified with a laser.arrow_forward
- What Art the Features of the Series of -omes? Define the following terms: a. Genome b. Transcriptome c. Proteome d. Metabolome e. Fluxomearrow_forwardPCR can be used ______. a. as a cloning vector b. in DNA profiling c. to modify a human genomearrow_forwardCloning Genes Is a Multistep Process The following DNA sequence contains a six-base sequence that is a recognition and cutting site for a restriction enzyme. What is this sequence? Which enzyme will cut this sequence? (See Figure 13.5 for help.) 5 CCGAGGAAGCTTAC 3 3 GGCTCCTTCGAATG 5arrow_forward
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