If you're looking for a great AI stock under $10… you need to watch this right away. What the company is doing is pretty incredible. It could end up saving billions of lives… and billions of dollars. In short, the company is the creator of the first AI-designed drug to enter clinical trials. And this is a huge deal. Normally, bringing a new drug to market takes an average of 10 years and between $2.5 and $12 billion. However, new AI technology has the potential to make the process up to 1000 times faster. The Wall Street Journal reports that “the time required for the early stages of drug discovery could shrink from years to months.” Not only that, it has the potential to develop “never-before-seen molecules that could treat diseases like pancreatic cancer or ALS.” In short, this is groundbreaking stuff. And this #1 AI company is at the forefront of all of it. Get it here.
CRISPR, which stands for “Clustered Regularly Interspaced Short Palindromic Repeats,” is a family of DNA sequences found in the genomes of prokaryotic organisms like bacteria and archaea.
These sequences are derived from past invaders such as viruses and serve as a kind of “memory system” for the organism.
When a known invader's DNA is detected, the CRISPR system can recognize and cut it, thereby neutralizing the threat.
The CRISPR system has been adapted for use in genetic engineering as a tool for editing genes.
The most commonly used form of this technology is CRISPR-Cas9, where “Cas9” refers to an enzyme that can cut DNA at a location specified by a guide RNA.
This allows for precise, directed changes to genomic structure and gene activity in a wide variety of organisms, including humans.
Today, we’re going to explore one CRISPR stock to buy under $10. It’s an exciting time to potentially invest in this technology because it has the potential to change the world in a ton of positive ways. Here’s how…
What Does CRISPR Do?
Gene Editing: The primary application of CRISPR is to modify genes for various purposes, ranging from basic research to potential treatments for diseases.
Functional Genomics Research: Researchers use CRISPR to understand the function of individual genes and how they interact within biological systems.
Agriculture: CRISPR is used to create genetically modified crops that are more resistant to pests, have longer shelf lives, or possess other desirable traits.
Biomedical Applications: CRISPR has the potential to treat a wide range of diseases, including genetic disorders like cystic fibrosis, muscular dystrophy, and even certain types of cancer.
Gene Drives: CRISPR can be used to create “gene drives,” which are designed to spread a particular genetic modification throughout a population rapidly.
Industrial Biotechnology: CRISPR can be used to engineer bacteria or yeast for the production of biofuels, plastics, and other chemicals.
Animal Research: CRISPR is used to create animal models of human diseases for research purposes.
Ethical and Social Implications: The power of CRISPR technology has also raised ethical questions, particularly concerning the potential for “designer babies” and the unintended consequences of gene editing.
Diagnostics: CRISPR-based diagnostic tools, like CRISPR-Cas12 and CRISPR-Cas13, are being developed to detect viral and bacterial infections.
Conservation: Some propose using CRISPR to bring back extinct species or to help endangered species by enhancing their resistance to diseases.
The technology is still relatively new, and while it has tremendous potential, there are also ethical and safety considerations that are the subject of ongoing debate and research.
One CRISPR Stock to Buy Under $10
Editas Medicine (EDIT) is a leading genome editing company that utilizes CRISPR technology to develop transformative genomic medicines designed to treat a broad range of diseases at the genetic level. Their approach is based on the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) systems. Some of their focus areas include:
Ocular Diseases: One of their lead programs is EDIT-101, which is being developed to treat Leber Congenital Amaurosis 10 (LCA10), a rare genetic illness that leads to blindness.
Hematopoietic Stem Cells: Editas is working on editing these cells to treat sickle cell disease and beta-thalassemia.
Immuno-Oncology: They are researching ways to modify T cells to make them more effective in fighting cancers.
Usher Syndrome: Another genetic disorder that affects both hearing and vision.
Research & Development: Editas Medicine continues to invest in the development of its proprietary genome editing platform to expand the range of genetic diseases it can target.
EDIT stock is currently trading for approximately $9 per share. The stock is down 45% in the last year, and 72.5% in the last 5 years.
Investors would be wise to avoid EDIT until we hear any breakthroughs. In the meantime, check this CRISPR stock out…
A famous A.I. billionaire recently took center stage and shocked the world.
He left the crowd utterly speechless.
But what exactly happened?
He revealed a breakthrough device that will change everything you know about making money.
You won't see this story on the nightly news.