Download Cell Transformation Chapter 13-3

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Epigenetics of human development wikipedia , lookup

Epigenomics wikipedia , lookup

Cancer epigenetics wikipedia , lookup

Neuronal ceroid lipofuscinosis wikipedia , lookup

Genomics wikipedia , lookup

Primary transcript wikipedia , lookup

Protein moonlighting wikipedia , lookup

Genomic library wikipedia , lookup

Epigenetics of diabetes Type 2 wikipedia , lookup

Genome evolution wikipedia , lookup

Gene expression profiling wikipedia , lookup

Gene nomenclature wikipedia , lookup

Molecular cloning wikipedia , lookup

Gene wikipedia , lookup

Polycomb Group Proteins and Cancer wikipedia , lookup

Nutriepigenomics wikipedia , lookup

DNA vaccination wikipedia , lookup

Genome (book) wikipedia , lookup

Extrachromosomal DNA wikipedia , lookup

Gene therapy wikipedia , lookup

Gene therapy of the human retina wikipedia , lookup

Cre-Lox recombination wikipedia , lookup

Plasmid wikipedia , lookup

Point mutation wikipedia , lookup

Genome editing wikipedia , lookup

Helitron (biology) wikipedia , lookup

No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup

Therapeutic gene modulation wikipedia , lookup

Designer baby wikipedia , lookup

Site-specific recombinase technology wikipedia , lookup

Microevolution wikipedia , lookup

NEDD9 wikipedia , lookup

Vectors in gene therapy wikipedia , lookup

Genetic engineering wikipedia , lookup

Artificial gene synthesis wikipedia , lookup

History of genetic engineering wikipedia , lookup

Transcript
Cell Transformation Chapter 13-3
I.
Bacterial Transformation – using a bacteria cell
to produce proteins from other organisms (ex.
Insulin for diabetics)
A. Bacterial DNA forms a round loop called a
Plasmid
B. Genetic Marker- can be a gene for antibiotic
resistance that is spliced onto the gene that
researchers want expressed.
1. Use a restriction enzyme to cut plasmid and
use same enzyme to cut out segment of
DNA
2. This creates ends with nucleotides that
match “sticky ends”
3. Allows bacteria with the gene to be
separated from bacteria that don’t
4. After bacteria cells reproduce the protein,
the protein can be removed and purified for
use
II.
Plant Transformation- A gene can be inserted
into a plant cell using a modified DNA
(bacterial) plasmid and an inactive tumor
producing gene.
III.
Animal Transformation- Using similar
techniques, genes can be inserted into animal
cells.