1a) If the PCR begins with 1 nanogram of target DNA, calculate how many grams of DNA would be present after 10 cycles of PCR.
1b) About how many DNA copies were made from the original DNA target if it were to go through 10 cycles of PCR. Answer in scientific notation.
1a) the PCR progress geometrically.
if we are starting with x amount of DNA
x, 2x, 4x, 8x....
this is like 1,2,4,8,16,32,64,128,256,512,1024
so after 10 cycles the amount of DNA=1024x
so amount of DNA after 10 cycles= 1
1024=1024
nanogram.
1b) If the PCR starts with 1 DNA molecule
the PCR progress as
1,2,4,8.....
this follows a geometric progression, the r=nth term/n-1 th term=4/2=2
number of DNA molecules after n cycles= n+1 th term
in a geometric progression n+1 th term = ar^n+1-1=ar^n
a is the first term, a=1
number of DNA molecules after 10 cycles= 1
2^10=1024
so the number of DNA molecules after 10 cycles of PCR if we are
starting with 1 molecule of DNA = 1024=1.024
10^3
1a) If the PCR begins with 1 nanogram of target DNA, calculate how many grams of...
A PCR reaction begins with 5 double stranded segment(s) of DNA. Part A: Estimate the number of double-stranded copies of DNA that are present after the completion of 15 amplification cycles? Part B: After 30 cycles?
Suppose you start a PCR reaction with 3 copies of a double stranded DNA fragment. How many copies will be present after 4 replication cycles? a. 7 b. 64 c. 48 d. 24 e. 8
Today we amplified 50 ng of Bos taurus (calf) DNA by PCR. This amount of DNA contains about 15,000 molecules of the insulin gene [50 ng DNA= 2.5 x 10-20mol; (2.5x10-20)x(6.023×1023) = 1.5 x 104molecules]. We performed PCR for 35 cycles to amplify the amount of this gene. a. What is the theoretical fold amount of DNA amplified by 35 cycles of PCR (remember the 2Nformula)? b. How many molecules of the insulin gene would, therefore, be present after PCR?
• 4. How many copies of the primers do you add to the PCR? You add 3 pl. of a 5 M solution of each primer, If you had 100 copies of the template DNA would there be enough primers to support 30 cycles of PCR? Remember the amount of template doubles (in theory) with each cycle. After 1 cycle there will be 2xthe starting amount, after 2 cycles 4 x the starting amount.
After 10 cycles of PCR, approximately how much DNA would you have starting with 10ng of the target region?
if you start with 2 pieces of DNA, after 4 cycles of PCR how many would you have?
1. Explain why, when PCR is used to amplify the same region of DNA from two different people, the size of the DNA fragment(s) generated may be different? 2. What characteristic of the DNA molecule makes it possible to use electrophoresis to separate DNA molecules by size? Explain why this characteristic is important for electrophoresis and what part of the DNA molecule creates this characteristic. 3. You are performing PCR. After four cycles of PCR, how many double-stranded copies of...
If you start with 47 DNA segments, how many total copies of DNA will you have after 12 cycles of PCR? Also what does attenuated mean in regards to the K12 strain of E. coli being used in lab? Is the answer “we have removed the gene that allows the bacteria to replicate”? Thank you!!
1.The PCR (polymerase chain reaction) protocol that is currently
used in laboratories was facilitated by the discovery of a
bacterium called Thermus aquaticus in a hot spring inside
Yellowstone National Park, in Wyoming. This organism contains a
heat-stable form of DNA polymerase known as Taq
polymerase, which continues to function even after it has been
heated to 95°C.
a.Why would such a heat-stable polymerase be beneficial in
PCR?
b.What would happen if it weren’t
heat stable?
c.How might you choose...
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