Why must some of your DNA be replicated in fragments? Please do not focus on how the DNA is replicated but tell me why some of it must be replicated in fragments.
DNA replication I'd directionAl it takesplace only in 5'-3' direction which is nothing but the direction of leading strand. Hence the replecation of the other synthesising strand that is lagging strand should takes place in opposite direction that is 3'-5'. But practically in lagging strand orientation 3'-5' replication doesn't occur. Hence DNA lagging strand folds to its back to form a loop at site of replication to cope up with leading strand direction and after finishing a small stretch of replication of lagging strand it unfolds to get its normal 3'-5' orientation and during this time replication pause for a while to leave a gap. After this it again form anot her loop forward to the previous one and replication begins. Like wise lagging strand folds back and forth to produce discontinuous mode of replication in the 5'-3' direction to produce small fragments, on the other hand leading strand shows continous replication to produce single stretch of DNA.
Why must some of your DNA be replicated in fragments? Please do not focus on how...
1 pt 1 Question 1 Why must one strand of DNA be replicated in fragments? DNA polymerase can only add 20 nucleotides in a strand and then must start over ODNA polymerase can only add nucleotides to the 3 hydroxyl of a growing strand O it would be too crowded for two DNA polymerases to be going in the same direction all of the above Question 2 1 pt the DNA would spin and possibly break while being opened in...
What are restriction enzymes and how do they affect DNA? Why do some fragments move quickly and some move slowly through an agarose gel? How can type II restriction enzymes and agarose gels be used to identify samples from individuals with the similar DNA sequence?
1. DNA Replication (10 Pts.) Create your own strand of dsDNA being sure to indicate 3’ and 5’ ends. Tell me how DNA is replicated including how bases pair. Show me DNA replication using your strand (this can be hand drawn). What enzymes are used to actually make the new DNA? How is the DNA primed for replication? What enzyme is responsible for this? What enzyme removes the primer and fills in the gap with DNA? What enzyme covalently bonds...
How do you calculate the average sizes and numbers of DNA fragments produced by digesting human genomic DNA with a given restriction enzyme?
the following Sequence of DNA was mixed with an unknown primer of length 15 BP, ddC, the four NTPs and DNA polymerase. the resulting mixture of DNA fragments were separated to provide fragments of lengths 23, 24, 28, and 32 BP amongst others (other fragments were observed but are not indicated). indicate below the sequence of the 15 bo primer from 5' to 3'. please explain how to do this d) The following sequence of DNA TTGCTCGACTGGACCTCACTGACACGA TCGCA TCCTTCGACTCGT was...
Describe the process of DNA replication in a well-organized manner. Start with the helicase and go through the entire process, step by step. Use these terms correctly: Helicase, DNA primase, single stranded binding proteins, DNA polymerase I, DNA Polymerase III, leading strand, lagging strand, okazaki fragments, ligase, topoisomerase, sliding clamp, clamp loader. Please use correct descriptions of the enzyme function. For example, do not say, “seals nicks.” Tell me what “seals nicks” means. If you speak about something you have...
1) If a restriction enzyme cuts a circular DNA into five fragments, how many restriction sites are there in the DNA? 2) How many molecules of DNA will be present after 6 cycles of PCR, if you started with one double-stranded DNA molecule? CELL BIOLOGY QUESTIONS!! SHOW WORK PLEASE
(blocked) d. PCR amplification of DNA fragments, cluster growth Below are some of the steps that occur in a Nextgen genomic sequencing reaction. Fill in the missing steps. Steps MUST be in the proper order. a. Isolate and fragment genomic DNA from an organism Ev [ Select ] Add primer/ fluorescent chain terminating nucleotides Bind to chip Assemble contig Remove chain terminator Read fluorescence Ligate linkers C e. (Select ] f. Wash away excess, non-bound chain terminating nucleotides [Select] h....
DNA Replication - Describe the process of DNA replication in a well-organized manner. Start with the helicase and go through the entire process, step by step. Use these terms correctly: Helicase, DNA primase, single stranded binding proteins, DNA polymerase I, DNA Polymerase III, leading strand, lagging strand, okazaki fragments, ligase, topoisomerase, sliding clamp, clamp loader. Please use correct descriptions of the enzyme function. For example, do not say, “seals nicks.” Tell me what “seals nicks” means.
Why do restriction enzymes need to be kept on ice? What order should the DNA, enzyme, water and buffer be added to the microcentrifuge tube for a restriction digest? If lambda DNA is linear, how many times would the enzyme have to cut the DNA to generate five DNA fragments? Would a shorter DNA fragment move faster or slower through the agarose gel than a longer fragment? Why?