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About Biomedical Basics
Biomedical Basics are AI-generated explanations prepared with access to the complete collection, human-reviewed prior to publication. Short and simple, covering biomedical and life sciences fundamentals.
Topics Covered
- Gene cloning & recombinant DNA
- Gene isolation methods
- Vector selection & design
- Restriction enzymes & ligase use
- DNA introduction into hosts
- Protein production & uses
- Biotech breakthroughs
- GMOs & therapeutic proteins
- Ethics & safety issues
Talk Citation
(2025, December 31). Gene cloning and recombinant DNA [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 31, 2025, from https://doi.org/10.69645/WUPI8265.Export Citation (RIS)
Publication History
- Published on December 31, 2025
Financial Disclosures
A selection of talks on Infectious Diseases
Transcript
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0:00
In this talk, we turn
our attention to
gene cloning and recombinant DNA
framing our discussion
around the core concepts and
laboratory processes of gene
cloning and recombinant DNA,
including gene isolation,
vector selection and
tools like restriction
enzymes and DNA ligase.
We will examine how recombinant
DNA is introduced into
host organisms enabling
protein production
for diverse applications
in medicine and industry.
The lecture will highlight
major breakthroughs such
as the creation of genetically
modified organisms and
therapeutic proteins as well as
address ethical and
safety considerations
that arise from these
transformative technologies.
We will explore the key
principles and processes that
underpin much of modern biology,
biotechnology and medicine.
Gene cloning enables precise
copying and manipulation of
DNA segments usually genes
by inserting them into host
organisms often bacteria.
We will discuss how genes are
isolated, cloned and expressed,
the biological tools involved,
major applications
in medicine and
agriculture and
the ethical considerations
of this technology.
Central to gene cloning is
isolating the gene of
interest from cellular DNA.
This can begin
with messenger RNA
using reverse
transcription to generate
complementary DNA
or directly from
genomic DNA via polymerase
chain reaction.
The isolated gene is then
inserted into a cloning vector,
a DNA molecule that
replicates in a host.
Common vectors include plasmids,