Options (A) and (C) are Incorrect in DNA Analysis
(A) DNA Fragments are Separated by Gel Electrophoresis, Not ELISA
Enzyme-Linked Immunosorbent Assay (ELISA) is a technique used for detecting and quantifying proteins, antibodies, and hormones, not for DNA separation.
Correct Technique: Gel Electrophoresis
The correct method for DNA fragment separation is gel electrophoresis, which works based on:
- Charge-based separation: DNA molecules are negatively charged due to phosphate groups.
- Size-dependent movement: Smaller DNA fragments migrate faster through the gel matrix.
- Use of agarose gel: Provides a medium for the DNA to travel when subjected to an electric field.
The movement of DNA fragments is described by the equation:
\( d \propto \frac{1}{\log M} \)
where:
- \( d \) = Distance traveled
- \( M \) = Molecular weight of the DNA fragment
Conclusion: Since ELISA does not separate DNA fragments, option (A) is incorrect.
(C) Recombinant DNA Technology Involves the Isolation of a Desired DNA Fragment
Recombinant DNA technology is a genetic engineering process that requires the precise isolation of a target DNA fragment before it can be inserted into a vector.
Steps in Recombinant DNA Technology:
- Isolation of DNA: Extracting the desired gene from the donor organism.
- Cutting DNA with Restriction Enzymes: Using molecular scissors to obtain the fragment.
- Insertion into a Vector: Ligating the DNA into a plasmid.
- Transformation: Introducing the recombinant DNA into a host cell.
- Selection & Screening: Identifying transformed cells.
Conclusion: Since isolation is a fundamental step, option (C) is incorrect.
Final Summary
- (A) is incorrect because DNA fragments are separated by gel electrophoresis, not ELISA.
- (C) is incorrect because recombinant DNA technology requires the isolation of the desired DNA fragment as an essential step.