In 1975, the Asilomar Conference on Recombinant DNA was organized by Paul Berg, a pioneer of recombinant DNA technology, at a conference center at Asilomar State Beach in California. Physicians, scientists, lawyers, ethicists, and others gathered to draft guidelines for safe applications of recombinant DNA technology. These general guidelines were adopted by the federal government and are still in practice today. Consider the implications of recombinant DNA as a new technology. What concerns might the scientific community have had then about recombinant DNA technology? Might those same concerns exist today?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
18. Molecular Genetic Tools
Genetic Cloning
Problem 11
Textbook Question
In the context of recombinant DNA technology, of what use is a probe?
Verified step by step guidance1
Understand that in recombinant DNA technology, a probe is a single-stranded DNA or RNA sequence that is complementary to a target sequence of interest.
Recognize that the probe is labeled with a detectable marker, such as a radioactive isotope or a fluorescent dye, to allow visualization after hybridization.
Use the probe to hybridize (bind) specifically to the complementary DNA or RNA sequence within a mixture of nucleic acids, enabling identification of the target sequence.
Apply the probe in techniques such as Southern blotting or Northern blotting to locate specific DNA or RNA fragments on a membrane after gel electrophoresis.
Interpret the presence and position of the probe's signal to determine whether the target sequence is present and to analyze its size or abundance.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Recombinant DNA Technology
Recombinant DNA technology involves combining DNA from different sources to create new genetic combinations. It is widely used in genetic engineering, cloning, and gene analysis to study or manipulate genes for research, medicine, and agriculture.
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DNA Probe
A DNA probe is a short, single-stranded sequence of nucleotides labeled with a detectable marker. It is designed to hybridize specifically to a complementary DNA sequence, allowing researchers to locate or identify particular genes or DNA fragments within a complex mixture.
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Hybridization in Molecular Biology
Hybridization refers to the process where complementary nucleic acid strands pair by base-pairing. In recombinant DNA technology, probes hybridize to target sequences, enabling detection or isolation of specific DNA segments through techniques like Southern blotting or in situ hybridization.
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