Question

In: Biology

When setting up a PCR experiment, you must prepare a positive control sample. What would the...

When setting up a PCR experiment, you must prepare a positive control sample. What would the positive control help you discover?

A) You forgot to add Loading Dye to your samples

B) The DNA ladder is denatured

C) Your thermocycler is broken

D) Your reagents are contaminated with foreign DNA

Solutions

Expert Solution

Answer and Explanation:

(D) Your reagents are contaminated with foreign DNA

In PCR, we use positive control sample which will always give the postive result for the test. We can compare our test results with positive control to infer the positive result. We also use negative control which is used to infer the negative result for the test.

For example in case of gene testing for cancer, a positive control sample will always gives results for the presence of mutated gene and a negative control sample will give negative results for the test (absence of mutation). We can compare our samples with positive and negative control to infer the results.

Suppose if positive control sample is producing a band at 200 bp and our sample produces a band which is very different from the positive control and produces a band at 500 bp or if it gives two or three bands it can be inferred that our reagents are contaminated with foreign DNA.

For other options,

If we did not add loading dye to the samples, the samples will not settle in the gel and also the tracking of the samples is not possible. If the DNA ladder is denatured, it will affect the calculation of size of the PCR product. If a thermal cycler is broken, even the positive control will not work.


Related Solutions

In a PCR experiment, what does it mean when the positive control has a DNA band,...
In a PCR experiment, what does it mean when the positive control has a DNA band, but the experimental tube does not?
1.) What is the positive control in this experiment? Negative control? Why do you think this?...
1.) What is the positive control in this experiment? Negative control? Why do you think this? Tube # 3 M Na Pyruvate(Activator) 0.1 M MgSO4 (activator) 0.1 M NaF (inhibitor) 5.0% Glucose (Activator) Water Fill With Co2 Produced after 40 min 1 - - - - 7.5 mL Yeast .10 mm 2 - - - 2.5 mL 5.0 mL Yeast 2.5 mm 3 - 5.0 mL - 2.5 mL - Yeast 5.0 mm 4 - - 0.5 mL 2.5 mL...
You are setting up a PCR reaction using DNA from a bacteria with a genome size...
You are setting up a PCR reaction using DNA from a bacteria with a genome size of 17 megabase-pairs (mb). How many nanograms of DNA will you need to add to the reaction to ensure there are at least 100 copies of the single gene you are trying to amplify? (assume the average molecular weight of a nucleotide pair is 650). (2 pt)
The thermal conductivity of a brass rod (property: thermal conductivity) when setting up an experiment to...
The thermal conductivity of a brass rod (property: thermal conductivity) when setting up an experiment to measure the thermal conductivity of a solid based on Fourier's Law, what hardware factors will need to be controlled? Give your reason for each one.
1. Compare PCR to qPCR, pros and cons 2. What must be considered when making PCR...
1. Compare PCR to qPCR, pros and cons 2. What must be considered when making PCR primers associated with annealing conditions? How to minimize errors when designing primers to anneal to the DNA template
If you would do a PCR experiment using the Klenow fragment of the E.coli DNA polymerase...
If you would do a PCR experiment using the Klenow fragment of the E.coli DNA polymerase I instead of Taq DNA polymerase, what would you have to change in the experimental set-up and explain why?
Which gene do we use as a positive control for PCR due to its presence in...
Which gene do we use as a positive control for PCR due to its presence in both granulocytes and monocytes, and its function as a "housekeeping" gene?
In an experiment, why would the concentration of a sample decrease when changing the wavelength for...
In an experiment, why would the concentration of a sample decrease when changing the wavelength for a spectrophotometer from 235 nm to 280 nm? This is just a general question, I would like to know why the absorbance peak would be higher at a wavelength of 235nm rather than at 280nm. Is this normal? or could it an experimetnal error?
Please prepare a tutorial on what positive definite means from the point of control systems engineering....
Please prepare a tutorial on what positive definite means from the point of control systems engineering. Provide an example how to calculate and determine this.
What is the difference between external and internal pricing? What factors must be considered when setting...
What is the difference between external and internal pricing? What factors must be considered when setting internal transfer pricing between divisions of a company? What are the different methods of setting internal transfer pricing? Which is the most effective? Why?
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT