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The pros of DNA technology involves the ability to insert particular traits in a species, production of artificial DNA, artificial production of important proteins and hormones, and DNA screening to detect hereditary disorders. The cons are; extinction of wild species caused by the rapid reproduction rate of artificial species, a process called genetic pollution, artificially produced species may show weaknesses, and the created species may carry new diseases.

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Q: What are some pros and cons of DNA technology?
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What are the pros and cons of gel electrophoresis?

Pros: The detection of DNA, RNA and proteins can be done using gel electrophoresis. Gel electrophoresis does not require a large amount of starting material. Cons: difficult to extract samples for further analysis. Harmful materials.


What are the pros and cons of integrating DNA microarray or chip technology into the forensic DNA laboratory?

Pros: High-throughput analysis: DNA microarrays or chips can analyze multiple DNA samples simultaneously, increasing efficiency. Increased information: Can provide information on multiple genetic markers, enabling more comprehensive analysis. Cost-effective: Allows for testing of multiple markers in a single assay, potentially reducing costs. Cons: Complexity: Requires specialized equipment and training, which may be costly and time-consuming to implement. Data interpretation: Results from microarray analysis may be complex and require specialized expertise for interpretation. Sensitivity: Microarray technology may have limitations in detecting low-level DNA samples compared to traditional DNA analysis methods.


What is difference between recombinant DNA technology and Polymerase chain reaction?

r DNA technology is technology of creating new combination of DNA. While pcr is one of techniques used in r DNA technology for amplification of perticuler DNA fragment


When did DNA Plant Technology end?

DNA Plant Technology ended in 2002.


DNA technology is being used to develop crop plants that are?

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Why was the discovery of restriction enzymes important to recombinant DNA technology?

Restriction enzymes are important in recombinant DNA technology because they can cut DNA at specific sequences, allowing for the precise insertion of genes into other DNA molecules. This technology made it possible to manipulate DNA sequences, creating recombinant DNA molecules that could be used for genetic engineering and gene cloning.


How does DNA technology transfer bacteria genes from cell to cell?

DNA technology will transfer bacteria genes from cell to cell.


What career combines DNA technology and medicine?

Pharmaceuticals combine DNA technology and medicine.


What is Pros and cons of using DNA microarray?

Pros: Allows for the simultaneous analysis of thousands of genes, providing a comprehensive view of gene expression patterns. Can identify biomarkers for disease diagnosis and prognosis. Cons: High cost associated with purchasing and maintaining equipment. Requires specialized training to effectively analyze and interpret data. Data analysis can be complex and may require bioinformatics expertise.


What is the substance required to cleave the vector DNA during recombinant DNA technology?

Restriction enzymes are the substances required to cleave the vector DNA during recombinant DNA technology. These enzymes recognize specific DNA sequences and cut the DNA at specific points, allowing for the insertion of foreign DNA fragments.


How is PCR and recombinant DNA technology similar?

PCR and recombinant DNA technology both involve manipulating DNA in the laboratory. PCR is a technique used to amplify specific DNA sequences, while recombinant DNA technology involves combining DNA from different sources to create a new DNA molecule. Both techniques have revolutionized the field of molecular biology and have numerous applications in research and biotechnology.