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Question: Given table gives an account of the differences between PCR and gene cloning. Which of the following...

Given table gives an account of the differences between PCR and gene cloning. Which of the following points shows the incorrect difference ?

ParameterPCRGene cloning
1. EfficientMoreLess
2. Apparatus RequirementDNARestriction enzyme, ligase, vector, bacteria cell
3. ManipulationIn vitroIn vitro and In vivo
4. costMoreLess
5. AutomationYesNo
6. Error probabilityLessMore
7. Time for a typical experiment2 to 4 days4 hours

a. 1 and 3
b. 4 and 6
c. 4 and 7
d. 4,7, and 8

Explanation

Solution

Gene cloning is the selection of particular DNA and keeps into bacteria in vivo to produce the desired genes. Whereas polymerase chain reaction is invitro condition, where amplification of specific required DNA sequence is done.

Complete answer:

Gene cloningPCR
In this gene amplification, method, rDNA is constructed and it introduced into bacteria to produce clones and it is done invivoIn this amplification method, the sequence of DNA required are produced invitro
It requires restriction enzymes, DNA ligase and vector DNA and bacteria requiredAlong with the DNA sequence that to be amplified, it requires RNA primers, the most able DNA polymerase and nucleotide bases.
One microgram of the DNA quantity is required at least.Nanogram of the DNA is enough
For re-isolation of amplified DNA from rDNA, restriction enzyme is requiredNo re isolation is required.
2 to 4 days required4 hours is enough.
Labour intensiveNo need of any labor intensives
More error possibilitiesLess errors
Automation neededNo automation required.

Hence, the correct answer is option (C).

Additional information:
The majority of PCR cycles depend on thermal cycling because, in this process reactants are exposed to thermal cycling and do repeated cycles of both heating and cooling which permit different temperature dependent reactions only, which include DNA melting, and enzyme dependent DNA replication.

Note: In case of gene cloning, amplified DNA is used for limited purposes, because control selection of DNA sequence but in case of polymerase chain reaction, amplified DNA is used for a number of conditions as there are very few error possibilities.