Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- How many molecules (target sequence copies) will be produced by 30 PCR cycles? Assume you start with only 1 copy of the target sequence (very unlikely)? Show your work!arrow_forwardDescribe the method of a PCR technique in which you can amplify fragments randomly? Briefly.arrow_forwardfellow lab worker brings you DNA containing what might be a similar gene in Leopard Geckos (XG). She asks you to see if you can amplify it using the same primers you used in frogs and the Bearded Dragon. You run the PCR and then analyze the product by running the DNA on an agarose gel. As a control, you run out the PCR product you amplified in Bearded Dragons and a DNA “ladder” of DNA pieces of known sizes. The gel results are shown below. Marker = DNA ladder; Lane A = Bearded Dragon PCR product; Lane B = Leopard Gecko PCR results. In the box below, determine the sizes of the PCR products shown in Lanes A & B. Size of Bearded Dragon PCR product: ______________________________ Sizes of Leopard Gecko PCR products: ______________________ yes or No - based on the results shown in the gel above – would you say the frog PCR primers for gene X amplified the same gene in the Bearded Dragon?arrow_forward
- If you were to sequence a human genome today, how would the sequencing differ from that done during the Human Genome Project? Choose only the best answer. You would still use Sanger sequencing. You would still assemble the sequencing reads into a genome using bioinformatics. You still need to clone the DNA fragments prior to sequencing them. All three of the other statements are true.arrow_forwardWhat is the purpose of including a PCR reaction with no added DNA? Isn’t this just a waste of expensive enzyme when we know that without template, you will not get any PCR products?arrow_forwardIf you performed PCR to amplify a gene region, and you began with 20 copies of double stranded genome, after 18 cycles, about how many double stranded copies of that region would you have (in theory)?arrow_forward
- Explain why PCR generates billions of products that are all the same sizearrow_forwardWhy do you detect mutations one at a time on PCR? Is there any way to detect multiple mutations in PCR at once?arrow_forwardExplain why exome sequencing can be almost as valuable as genome sequencing. (Explain in your own words)arrow_forward
- Here is a DNA agarose gel showing PCR products from a mouse genotyping experiment. Genotyping tells us whether each mouse is a wild type mouse (i.e. not genetically modified) or a mutant mouse. Interpret the results for each mouse 1-3.arrow_forwardIn 1993, Kary Mullis won the Nobel Prize in Chemistry for his invention of the PCR process. Describe the three steps in each cycle of a PCR reaction. Why was the discovery of a thermostable DNA polymerase so important for the development of PCR?arrow_forward
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