Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Question
The human genome is made from more than 3 billion
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1 |
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13 |
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1,000 |
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1,000,000 |
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- Answer this question please.arrow_forwardA health provider contacts you regarding a specific patient. They ask you to sequence this patient’s DNA and sends you her blood sample. You split the patient’s blood sample into three equal parts. With each part, you perform three different protocols of DNA extraction and purification. You analyze the resulting DNA using the nanodrop. Protocol A260/280 ng/ul DNA Total volume (ul) 1 2.02 50 60 2 1.45 156 200 3 0.30 300 120 d)Halfway through the electrophoresis of your gel you realized that rather than using a buffer to make up your gel, you actually used distilled water. Do you think this mistake would alter the outcome of your gel electrophoresis? Explain. e) If you added your DNA to a well in a gel without first mixing it with gel loading solution, would this impact the final results? Explain. f) Only after the run you realize that you forgot to add ethidium bromide to the gel. What will happen to your sample? What could you do to the gel after the run?arrow_forwardThe current state-of-the-art in forensic DNA profiling involves the PCR-amplification and analysis ofshort tandem repeats, STRs, in the human genome. This approach has many distinct advantages.Please list and explain three of those advantages.arrow_forward
- Humans have very similar DNA sequences, with approximately 999/1000 letters being ide One possible way of telling the difference between these very similar sequences is by: Genetic engineering Analyzing RFLPS using gel electrophoresis Comparing the total amount of DNA from two or more peoplearrow_forwardWhat is DNA fingerprinting? Mention its application.arrow_forward. Lane 1 represents DNA taken from the murdered victim. Lane 2 through 5 are DNA samples taken from suspects in the crime. Lane 6 is from a bloodstain found near the victim. Q6. Why is it important to include the DNA taken from the murdered victim (Lane 1) in this DNA analysis?arrow_forward
- Many times a forensic scientist has only a single hair or a single drop of blood for analysis. The amount of DNA in this kind of material is very tiny, and is not enough to use for comparison. In other words, running a single experiment to compare the DNA in a drop of blood with several suspects would use up all of the DNA in that drop of blood. This could be a serious problem if none of the suspects provided a match. How would a forensic scientist increase the amount of DNA available to them, starting with the DNA that would be found in their crime scene sample, such as a drop of blood from a suspect? PCR RFLPS Gel electrophoresis STRSarrow_forwardSomeone broke into the bookstore and stole thousands of dollars’ worth of textbooks. Some hairs were left behind, from which DNA was extracted. An individual was caught with all five of the stolen textbooks in his bag. He claims his friend gave them to him. You decide to amplify two regions of the DNA (two loci, plural of locus) and digest the samples, and get the following result on the electrophoresis gel.L = Standard marker 1 = Suspect 1 2 = Suspect 2 3 = DNA from crime scene (Note: assume bands that are close in distance traveled are the same length. Higher concentrations of DNA can make a band appear to travel farther.) Which band patterns are similar?arrow_forwardWhich of the following statements is/are true? Choose only the best answer. Repetitive DNA can influence the appearance of an organism. Simple sequence DNA, transposable elements, and large-segment duplications are examples of repetitive DNA. Repetitive DNA can be useful in genetic profiling. All three of the other statements are true.arrow_forward
- Which of the following criteria do you feel is the most important one to optimize for a DNA profiling methods? Speed Discriminating power Sensitivity Cost False Positive Ratearrow_forwardHow to find any evidence of cantamination or degradation of DNA in the DNA profiles you examined? how important is the detabase that is used to determine allele frequencies in DNA profiling casesarrow_forwardBamHI KpnI SpeI XhoI PatI HindIII 400 500 200 300 700 NotI 75 2580 ECORI Frog DNA BamHI 575 KpnI HindIII 625 2150 HindIII 700 PstI clal 750 РКАВОО 2700bp 915 1900 SpeI AluI 1050 1525 BamHI ori You wish to make a recombinant DNA molecule that will contain one piece of pKABOO vector DNA and one piece of frog DNA so that you can clone a segment of frog DNA. You want cells containing your recombinant plasmid to be amp' and tet and you want to use enzymes that cut within the insertional marker gene. (Note that tet means that there is no functional tet gene in the plasmid.) Be sure that your plasmid has the ability to replicate autonomously in a bacterial cell. You do not have to include the entire frog DNA given below in your recombinant plasmid. Restriction enzymes would be used to clone segment of frog DNA The size of the recombinant plasmid is bp. The recombinant plasmid when transformed into E. coli confers resistance to which of the following antibiotics: Oampicillin only Otetracycline…arrow_forward
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