S/whatis the difference between SPM andAFM?// what is polymerase chain reaction (PER) ?• Show properties?

Introduction: The polymerase chain reaction was developed by Karry Mullis in the year 1983. It is…

Answered: S/what is the difference between SPM…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Similar questions

High Frequency Recombination results in which of the following? O 1) Plasmid DNA incorporated into the cell 2) Genomic DNA incorporated into the cell 3) Viral DNA incorporated into the cell 4) Plasmid and genomic DNA from the donor cell is incorporated into the recipient cell's genome 5) The movement of genes within the cell through homologous recombination
You have two samples you have to sequence: one is a cloned plasmid that you want to verify the sequence of, and another is the cDNA library of the transcriptome of a cell. Which method would you use for each sample and why?
The exponential nature of PCR allows spectacular increases in the abundance of a DNA sequence being amplified. Consider a 10-kbp DNA sequence in a genome of 1010 base pairs. What fraction of the genome is represented by this sequence; i.e., what is the fractional abundance of this sequence in this genome? Calculate the fractional abundance of this target sequence after 10, 15, and 20 cycles of PCR, starting with DNA representing the whole genome and assuming that no other sequences in the genome undergo amplification in the process.
In a PCR assay, what's the purpose of each temperature step at: -heating the sample to 50 C -heating the sample to 72 C -heating the sample to 95 C options to match: - allows primers to anneal to the template DNA - promotes synthesis of new DNA - separates the DNA strands in the samples
The exponential nature of PCR allows spectacular increases in the abundanceof a DNA sequence being amplified. Consider a 10-kbp DNA sequence in agenome of 1010 base pairs. What fraction of the genome does this sequence represent? That is, what is the fractional abundance of this sequence in this genome?Calculate the fractional abundance of this target sequence after 10, 15, and 20 cycles of PCR, starting with DNA representing the whole genome and assuming that no other sequences in the genome undergo amplification in the process.
Outline the essential steps in the polymerase chain reaction.
Which of the following are major differences between DNA and RNA polymerases? RNA polymerase, but not DNA polymerase, requires a primer to begin synthesizing the nucleic acid polymer DNA polymerase, but not RNA polymerase, requires a primer to begin synthesizing the nucleic acid polymer RNA polymerase, but not DNA polymerase, is unique to eukaryotic cells DNA polymerase, but not RNA polymerase, is unique to eukaryotic cells DNA polymerase is involved in replication; RNA polymerase is involved in transcription 00
Put the steps of one PCR cycle in the correct order: The PCR reaction mixture is heated to about 70 degrees, which is the optimum temperature for the polymerase to build the new strands of DNA, starting at the 3' end of the primer. The PCR reaction mixture is heated to 95 degrees Celsius, which denatures the double stranded template DNA. The PCR reaction mixture is cooled to about 50-55 degrees, which allows the primers to find their complementary site on the template and "anneal" the
Which of the following is true about restriction endonucleases?a) Type I and II requires ATP to move along DNAb) Type I, II and III requires ATP to move along DNAc) Type II requires no ATP and cleaves DNA within recognition sequenced) Type II requires ATP and cleaves DNA within recognition sequence
Find out whether the following are true or false. a)Klenow polymerase is E. coli DNA polymerase I which has no 5' → 3‘ exonuclease activity. b)The best way to increase the amount of the product in PCR amplification is to increase the cycle number. c)In a PCR, primers must be identical to their template strand in order for hybridization to occur. d)The accuracy of the amplification with Taq DNA polymerase is very high due to its high 3’→ 5’ exonuclease activity
Mention different roles & applications of polymerase chain reaction. Please briefly explain at your own words.
Choose the correct statements from the list below. There may be more than one correct statement. A) If you start with 2 DNA templates, after four rounds of PCR you'll have 32 copies B) PCR is useful in making millions or billions of copies of a gene so that it is present in a quantity large enough to study C) quantitative PCR is very similar to PCR, but fluorescent probes are added so that we can measure how much PCR product exists by examining how much the reaction fluoresces D) In real-time reverse transcriptase PCR, the RNA is used as a template to make a cDNA copy (through reverse transcriptase)

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S/what is the difference between SPM and AFM² // what is polymerase chain reaction (PCR) ? Show properties?