Technology or method
Recombinant DNA
DNA joined from different sources, the starting point of genetic engineering and of medicines such as recombinant insulin.
Using living systems to make medicines, tools and food.
Biotechnology uses living things and their molecules to make useful products, like medicines and medical tests.
It includes recombinant DNA, PCR, sequencing, gene editing, gene therapy and mRNA vaccines, each with its own benefits, risks and rules.
Modern biotechnology combines molecular tools with clinical and regulatory science. Here each technology is labeled established or emerging and linked to its primary sources.
Technology or method
DNA joined from different sources, the starting point of genetic engineering and of medicines such as recombinant insulin.
Technology or method
The polymerase chain reaction copies a chosen stretch of DNA millions to billions of times.
Technology or method
Reading the order of the bases in DNA, from single genes to whole genomes.
Technology or method
A bacterial immune system that researchers adapted into a programmable tool for cutting chosen DNA sequences.
Technology or method
Making targeted changes to DNA in living cells. Newer base and prime editors change letters without cutting both strands.
Technology or method
Treating disease by adding, repairing or switching off genes in a patient's cells.
Technology or method
Vaccines that deliver mRNA instructions for a pathogen protein. Modified nucleosides help the mRNA avoid an unwanted immune alarm.
Technology or method
Identical antibodies made by cultures descended from a single fused cell, used in research, diagnostics and medicine.
Technology or method
Producing a genetically identical copy. Dolly the sheep, reported in 1997, was cloned from an adult cell.
Structure
Cells that can renew themselves and give rise to specialized cells. Adult cells can be reprogrammed into stem-cell-like iPS cells.
Ethics and safety
Weighing the benefits, risks and fairness of biological research and its uses.
Ethics and safety
Risk-based practices and containment that protect people and the environment when working with biological agents.
Timeline and explorer
A sourced timeline from the double helix to CRISPR therapies, eight technologies labeled established or emerging, and a PCR model.
Simulation
Pair bases, follow a real human gene from DNA to protein, make mutations, and predict inheritance with Punnett squares.
Interactive explorer
Compare bacteria, archaea, fungi, protists and viruses side by side, and model how a bacterial culture grows.
Search published papers and preprints in Biotechnology, with clear labels for reviews, primary research, clinical trials and preprints.
Search papers in BiotechnologyThe explanations on this page are our own summaries of these sources. Follow a link to read the original; if anything here disagrees with it, the original wins. How we choose and check sources.
National Human Genome Research Institute. Talking Glossary of Genomic and Genetic Terms. National Human Genome Research Institute, NIH.
World Health Organization (2021). WHO publications. World Health Organization. Published 2021-07-12.
National Academies of Sciences, Engineering, and Medicine (2017). The National Academies Press.
Cohen SN, Chang AC, Boyer HW, et al. (1973). Proceedings of the National Academy of Sciences 70:3240-3244.
Recombinant plasmids that replicate in bacteria.
Johnson IS (1983). Science 219:632-637.
National Human Genome Research Institute. Talking Glossary of Genomic and Genetic Terms. National Human Genome Research Institute, NIH.
Saiki RK, Gelfand DH, Stoffel S, et al. (1988). Science 239:487-491.
PCR with heat-stable Taq polymerase.
Sanger F, Nicklen S, Coulson AR (1977). Proceedings of the National Academy of Sciences 74:5463-5467.
Nurk S, Koren S, Rhie A, et al. (2022). Science 376:44-53.
The Telomere-to-Telomere consortium's gapless human genome assembly.
National Human Genome Research Institute. Talking Glossary of Genomic and Genetic Terms. National Human Genome Research Institute, NIH.
Barrangou R, Fremaux C, Deveau H, et al. (2007). Science 315:1709-1712.
Jinek M, Chylinski K, Fonfara I, et al. (2012). Science 337:816-821.
Showed Cas9 can be programmed with guide RNA to cut chosen DNA sequences.
Cong L, Ran FA, Cox D, et al. (2013). Science 339:819-823.
Komor AC, Kim YB, Packer MS, et al. (2016). Nature 533:420-424.
Anzalone AV, Randolph PB, Davis JR, et al. (2019). Nature 576:149-157.
U.S. Food and Drug Administration. fda.gov. U.S. Food and Drug Administration.
National Human Genome Research Institute. Talking Glossary of Genomic and Genetic Terms. National Human Genome Research Institute, NIH.
U.S. Food and Drug Administration (2023). FDA News Release. U.S. Food and Drug Administration. Published 2023-12-08.
Approval of Casgevy (CRISPR-based) and Lyfgenia for patients 12 and older.
Karikó K, Buckstein M, Ni H, et al. (2005). Immunity 23:165-175.
Modified nucleosides reduce innate immune recognition of synthetic mRNA.
Polack FP, Thomas SJ, Kitchin N, et al. (2020). New England Journal of Medicine 383:2603-2615.
Baden LR, El Sahly HM, Essink B, et al. (2021). New England Journal of Medicine 384:403-416.
Köhler G, Milstein C (1975). Nature 256:495-497.
The hybridoma method for monoclonal antibodies.
Wilmut I, Schnieke AE, McWhir J, et al. (1997). Nature 385:810-813.
Takahashi K, Yamanaka S (2006). Cell 126:663-676.
World Health Organization (2021). WHO news release. World Health Organization. Published 2021-07-12.
World Health Organization (2020). WHO publications. World Health Organization. Published 2020-12-21.
Centers for Disease Control and Prevention, National Institutes of Health. CDC Laboratories. U.S. Department of Health and Human Services.
The U.S. reference for laboratory biosafety practice.
Berg P, Baltimore D, Brenner S, et al. (1975). Proceedings of the National Academy of Sciences 72:1981-1984.
Scientists' own guidelines for the safe conduct of recombinant DNA research.