1. You order two primers from a company that synthesizes oligonucleotides. Theprimers have the exact same G and A content, but arranged differently.Primer 1 = GAGAGAGAGAGAGAGAGAGAPrimer 2 GGGGGGGGGGAAAAAAAAAA=a) Which one would you expect to have the higher melting point? Explain.b) Based on your answer to (a), draw a melting curve for primer 1 (line) andprimer 2 (dashed line). Be sure to label the axes, and the Tm.c) What does the Tm represent? Draw what you would expect Primer 2 to looklike at the Tm.

Primers are short stretches of nucleotides that are used to initiate the synthesis of nucleic acids.…

Answered: 1. You order two primers from a company…

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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By average, how many Sau3A (5’GATC3’) sites are there in a 10 kd DNA molecule? (1/4)^6 * 10,000 = 2.44140625 => 2.4 For the above 10 kb DNA, if you use Sau3A to do a complete digestion, you will only get a lot of small fragments ( 200~500 base pairs). What should I do if I want to get larger digested fragments (say 3 to 5 kb) Please answer asap and type your answer and do not copy from anywhere please
Figure 2 illustrates a type of gene mutation. a) State the type of gene mutation shown in Figure 2. b) Name the genetic disorder that would arise from this mutation. c) What is the difference(s) between gene mutation shown in Figure 2 from a frameshift mutation?
Please choose the correct answer. Thank you!
2. Sanger sequencing question. a). Why the Sanger sequencing chemistry would not work if too much ddNTP is added in the reaction mixtures? if we have too much ddNTP present in our reaction, we would have early termination near their 5' end and we would never generate products that are long enough to determine the sequence in the capillary electrophoresis. b) In a modified Sanger sequencing experiment, products from each reaction were recovered after separation by gel electrophoresis, and their exact molecular masses were determined by mass spectroscopy for the molecular species where all phosphodiesters are ionized. The molecular ions were found as follows: A reaction: 1163, 3050 and 3363; C reaction: 1451 and 3651; G reaction: 1779, 2107, and 2435; T reaction: 2738 and 3954. The reactions used d(AGC) as a primer. What is the sequence of the target DNA? show/explain your work.
The DNA of a deletion mutant of λ bacteriophage has a length of 15.4383 μm instead of 19.6356 μm. How many base pairs are missing from this mutant? *
1.(a) what are the possible secondary structures of the primer and what are there explain with illustration. (b)why is annealing temperature important and how it is connected to melting temperature?
1) Prepare the following enzymatic reaction, present it in tabulated form. In a final volume of 30 ul, where buffer 4 (10 ml). How much volume of each reagent would be used and how much of water? Is there any problem? 2) The DNA pol 1 enzyme comes at a concentration of 50,000 U/ml. You have to prepare a 50 ug PCR reaction where you must use 0.05 U/ml reaction. You add 10 ul of PCR buffer, 2 ng of tempered DNA that is at a concentration of 0.5 ng/ul, primers (which are at 200 mM) so that each one remains at a concentration of 200 uM, Mg+2 that is 5 mM (10 X), enzyme and water. Present the table of all the reagents included in the reaction, the volumes of each one in ul. Present where the initial and final concentration of each reagent applies. Assume you have micropipettes for all values.
Below is an EMSA showing four different reactions, A-D. In each tube there is some combination of labelled DNA probe, Protein X (the protein you are studying), and an antibody for Protein X. Identify which combination of components are found in each of the four reactions and explain how you determined that based on the molecular interactions being studied and your knowledge of gel electrophoresis. It is possible that multiple lanes have the same component(s). A B C D EMSA
H2N 1.) Look carefully at this nucleotide: N: N- Но-Р-О OH a.) Number the carbons in the sugar group. (Remember the "prime" symbols.) b.) Is this a purine or a pyrimidine? How do you know? c.) Would this nucleotide be used for DNA or RNA? How do you know? (Be specific.) d.) Is this nucleotide ready to be used for DNA replication or RNA transcription? Why/why not? e.) If this nucleotide were incorporated into a growing DNA or RNA strand, where would the next added nucleotide be attached to this one?
5- ddNTP differs from dNTP in..... and N is representing.. a) The first has no OH in both C 1,2, but dNTP has OH in C3 of the sugar/A, G.T.C. b) The first has no OH in both C 2 & 3, but dNTP has OH in C3 of the sugar/the bases. c) ddNTP is used to stop DNA elongation / nitrogen d) ddNTP has only one OH in C3/A,G,T.,C
For the following sequence please design an 18 base pair forward primer. ATGGCTGATAAGATAGAGAGGCATACTTTCAAGGTCTTCAATCAAGATTTCGAAAAAGAGCTGGAGTTTGGATTAGATAGAAAATATTTTTAG
Which of the following sequences is less favorable to find in a folded beta? Select one: a.l-V-A-I-G-P-L-A-V-F-Y b. G-A-L-V-F-C-V-I-L-L-P c. E-V-A-I-I-F-M-D-G-V-A d. A-V-G-I-L-P-L-A-V-F-Y e.A-A-V-L-L-A-I-G-L-M-W

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