
Explore the extremes of genetic engineering and learn to use data visualization to understand topics, increase your comprehension, and apply the concepts practically.
Discover Arthur Kornberg's DNA copying and Paul Burke's DNA transfer techniques, and observe how sequencing and protein synthesis underpin the genetic basis of living cells.
Explore biochemistry foundations in genetic engineering, from glucose metabolism and phosphorylation to calcium homeostasis, vitamin D regulation, and protein structure with active sites and alternative splicing.
Explore animal cell structure, including nucleus, chromatin, nuclear envelope, ribosomes, endoplasmic reticulum, cytoskeleton, and vesicles, through fluorescence microscopy and 2D/3D views, linking cell biology to genetic engineering foundations.
Explore enzyme technology within genetic engineering, including dehydrogenase activity and the synthesis of chemical factors essential to oxygen binding, with illustrative examples.
Explore genetic engineering through genetics and cytogenetics, linking clinical concepts such as skin biopsy and protein divergence to understand human genetic variation.
Explore immunology fundamentals related to genetic engineering, including activation of APCs, immunofluorescence with antibodies, plasma membrane roles, and basics of immunotherapy.
Explore the fundamentals of genetic engineering within molecular biology, including DNA transcripts and translation, to understand how genes drive cellular processes.
Explore how applied physics informs biophysics concepts, including electrostatic forces and coordination between parts, with visual graphics and historical posters as study aids.
Engineers design recombinant proteins, including fusion proteins and growth hormones such as follicle-stimulating hormone, with extended examples illustrating their applications in genetic engineering.
Gene therapy uses engineered cells to produce therapeutic proteins, delivered to patients to act inside the body, with culture and production steps performed outside the body.
Genetics is a branch of biology concerned with the study of genes, genetic variation, and heredity in organisms.
Genetic processes work in combination with an organism's environment and experiences to influence development and behavior, often referred to as nature versus nurture. The intracellular or extracellular environment of a living cell or organism may switch gene transcription on or off. A classic example is two seeds of genetically identical corn, one placed in a temperate climate and one in an arid climate (lacking sufficient waterfall or rain). While the average height of the two corn stalks may be genetically determined to be equal, the one in the arid climate only grows to half the height of the one in the temperate climate due to lack of water and nutrients in its environment.
Molecular genetics
DNA, the molecular basis for biological inheritance. Each strand of DNA is a chain of nucleotides, matching each other in the center to form what look like rungs on a twisted ladder.
Although genes were known to exist on chromosomes, chromosomes are composed of both protein and DNA, and scientists did not know which of the two is responsible for inheritance. In 1928, Frederick Griffith discovered the phenomenon of transformation (see Griffith's experiment): dead bacteria could transfer genetic material to "transform" other still-living bacteria. Sixteen years later, in 1944, the Avery–MacLeod–McCarty experiment identified DNA as the molecule responsible for transformation.The role of the nucleus as the repository of genetic information in eukaryotes had been established by Hämmerling in 1943 in his work on the single celled alga Acetabularia.The Hershey–Chase experiment in 1952 confirmed that DNA (rather than protein) is the genetic material of the viruses that infect bacteria, providing further evidence that DNA is the molecule responsible for inheritance.
James Watson and Francis Crick determined the structure of DNA in 1953, using the X-ray crystallography work of Rosalind Franklin and Maurice Wilkins that indicated DNA has a helical structure (i.e., shaped like a corkscrew).Their double-helix model had two strands of DNA with the nucleotides pointing inward, each matching a complementary nucleotide on the other strand to form what look like rungs on a twisted ladder.