The CRISPR Genetic Technology

The CRISPR Genetic Technology

The CRISPR entails gene editing tools used by scientists to alter the current state of organisms. The scientific method used in the laboratory to develop CRISPR involves the repetition of a sequence of genetic codes while interfering the process with remnants of past invaders genetic codes. The hypothesis was a study of orthologous categories of proteins through complex analysis hence the rationale to identify if the bacteria immune system is based on insert homologous can phage DNA in the array of natural pacers (Haselkorn 4). Experimentation was done to show how the CRISPR responds to phage attack in the processes of producing yogurt. Therefore, the experiment was done in the dairy industry in yogurt processing. In the test, the CRISPR proved to be an adaptive immune system.

Despite the fact the CRISPR has various benefits such as curing the ailing genes to transplants of organs, they have long-term effects which might interfere with the well-being of people. The CRISPR is used to treat cancer(Frischkorn 1005). The new technology can be used to develop immunotherapies used in the diagnosis of cancer.  The immunotherapy is done through the application of T-cells. The technology can be used to eliminate any genetic diseases that affect people. Scientists used the new technology to cure faulty genes which cause conditions such as diabetes that are genetic.

The CRISPR also raises concerns on the germ-line cells. With the scientific modification of human embryos and reproductive cells such as sperms, the changes are transferrable to the next generations; thus traits such as stiff muscles will affect the future generations.

Works Cited

Frischkorn, Kyle. “A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution.” Science 356.6342 (2017): 1005-1006.

Haselkorn, Robert. “A Crack At CRISPR: A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution by Jennifer A. Doudna and Samuel H. Sternberg Houghton Mifflin Harcourt, Boston, 2017.” (2017): 3-4.

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