Report Description

Forecast Period

2025-2029

Market Size (2023)

USD 2.40 Billion

CAGR (2024-2029)

16.28%

Fastest Growing Segment

Service Segment

Largest Market

North America


Market Overview

Global CRISPR and Cas Genes Market was valued at USD 2.40 Billion in 2023 and is anticipated to project robust growth in the forecast period with a CAGR of 16.28% through 2029. The CRISPR technology improves the therapeutic efficacy of modified T-cells for the treatment of various malignancies. Additionally, the development of chimeric antigen receptor T (CAR-T) cells is strongly related to cancer treatment. In May 2022, Caribou Biosciences, Inc. presented data on the mechanism underlying the potential of chRDNA genome-editing technology in primary human T cells. It provides a reproducible and robust technique to boost the specificity of genome editing, and it improves the efficacy of allogeneic cell therapies. These developments are anticipated to drive the growth of the market in the coming years.

Key Market Drivers

Advancements in Genetic Research

As genetic research advanced, scientists gained a deeper understanding of gene functions and their implications for health and disease. This knowledge drove the demand for precise and efficient gene editing tools like CRISPR-Cas, which allowed researchers to target specific genes and investigate their functions. Genetic research unveiled the potential of CRISPR-Cas technology for therapeutic applications. The ability to edit genes opened up new avenues for treating genetic disorders, inherited diseases, and even some acquired conditions. Research into gene therapies and personalized medicine heavily relied on CRISPR-Cas technology. Genetic research advancements facilitated the identification of novel drug targets and biomarkers. CRISPR-Cas systems played a pivotal role in the validation of these targets, aiding in the development of more effective and targeted drugs. This integration of genetic research and CRISPR-Cas technology accelerated the drug discovery process. Genetic research led to the discovery of key genes responsible for desirable traits in crops, such as disease resistance, improved yield, and nutritional content. CRISPR-Cas systems were utilized to modify these genes, leading to the development of genetically modified organisms (GMOs) with enhanced agricultural traits. Genetic research advancements supported the growth of biotechnology industries. The use of CRISPR-Cas technology in industrial biotechnology, such as biofuel production and enzyme optimization, gained momentum due to the improved understanding of gene functions and regulatory mechanisms. Advances in genetic research increased the demand for high-quality research tools, including CRISPR-Cas reagents and kits. As researchers across various fields sought to leverage gene editing technology, the market for CRISPR-Cas-related products and services expanded. The promising outcomes of genetic research and CRISPR-Cas applications attracted substantial investment from both public and private sectors. Collaborations between academic institutions, biotechnology companies, and pharmaceutical firms aimed to further develop and commercialize CRISPR-Cas-based products.

Rising Demand for Gene Therapies

Gene therapies involve the modification of an individual's genetic material to treat or prevent diseases. CRISPR-Cas technology provides a precise and efficient way to edit genes, making it a valuable tool for developing targeted gene therapies. The demand for CRISPR-Cas technology increased as researchers and pharmaceutical companies sought to develop therapies for genetic disorders that were previously difficult to address. The ability to edit genes using CRISPR-Cas systems opened opportunities to develop innovative treatments for a wide range of diseases, including inherited genetic disorders, cancer, and rare diseases. The rising demand for these cutting-edge therapies drove the growth of the CRISPR and Cas genes market, as biotech companies and research institutions invested in developing and commercializing these treatments. Gene therapies often involve personalized approaches, where treatments are tailored to an individual's unique genetic makeup. CRISPR-Cas technology's precision allowed for the customization of therapies based on a patient's specific genetic mutations, increasing the effectiveness and safety of treatments. This personalized approach contributed to the growing demand for CRISPR-Cas technology. The rising interest in gene therapies led to increased investment and funding in the biotechnology and pharmaceutical sectors. Companies working on CRISPR-Cas technology and gene editing saw higher levels of investment as investors recognized the potential for groundbreaking medical advancements. The demand for gene therapies prompted regulatory agencies to establish guidelines and regulations for their development and approval. The regulatory framework influenced how CRISPR-Cas technology was used in clinical settings and commercial applications, shaping the growth trajectory of the market. Pharmaceutical companies, biotech startups, and academic institutions forged partnerships and collaborations to advance the development of gene therapies. These collaborations often included the utilization of CRISPR-Cas technology, which played a pivotal role in accelerating research and development efforts.

Rising Drug Discovery and Development

One of the early stages in drug discovery involves identifying potential therapeutic targets, which are often specific genes or proteins implicated in diseases. CRISPR-Cas technology has been instrumental in validating these targets by enabling researchers to efficiently manipulate and study genes to understand their functions and effects on disease pathways. CRISPR-Cas technology has been integrated into high-throughput screening processes to identify potential drug candidates. By using CRISPR to create gene knockouts or modifications, researchers can assess the impact of these changes on disease-related phenotypes, allowing for the rapid identification of promising compounds. CRISPR-Cas technology has enabled the creation of cellular and animal models that closely mimic specific diseases. These models are crucial for studying disease mechanisms, testing potential drug candidates, and understanding how genetic modifications affect disease progression. Genetic mutations can lead to drug resistance in various diseases, including cancer. CRISPR-Cas technology helps researchers understand the genetic basis of drug resistance, allowing for the development of strategies to overcome it and enhance the effectiveness of treatments. Before a potential drug candidate can move into clinical trials, it undergoes rigorous preclinical testing. CRISPR-Cas technology is used to validate the target's role in disease progression and to assess the potential effects of candidate drugs on gene expression and function. The integration of CRISPR-Cas technology in drug discovery and development processes has expedited research timelines. It enables more efficient testing of hypotheses, quicker validation of drug targets, and faster identification of lead compounds. The use of CRISPR-Cas technology in drug discovery has prompted discussions around regulatory guidelines and safety concerns. Clear regulations are essential to ensure that the technology is used responsibly and ethically in the development of new therapies.


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Key Market Challenges

Ethical and Regulatory Concerns

One of the most significant ethical concerns surrounding CRISPR-Cas technology is the potential for human germline editing, which involves making heritable changes to the genetic material of embryos. This practice raises ethical dilemmas about altering the human germline and introducing potential unintended consequences. Many countries and regulatory bodies have placed restrictions on germline editing, impacting the commercial viability of related applications. Despite its precision, CRISPR-Cas technology can sometimes cause unintended genetic modifications in regions other than the target site. This raises concerns about the safety and potential long-term effects of gene editing. Regulatory agencies require thorough assessment of off-target effects before any CRISPR-based therapies can move forward, potentially delaying their development. In clinical trials involving gene editing, ensuring informed consent from patients is crucial. Ethical considerations arise when patients might not fully understand the risks, benefits, and long-term implications of the experimental therapies. Striking a balance between advancing medical science and respecting patient autonomy can be challenging. The potential for CRISPR technology to be used for unintended or unethical purposes, such as creating dangerous pathogens or bioweapons, has led to discussions about appropriate regulations and safeguards. Balancing scientific progress with the need for responsible oversight is a challenge. The complex patent landscape surrounding CRISPR technology has led to legal disputes between research institutions and companies. These disputes can slow down research and commercialization efforts and create uncertainty in the market.

Lack of Predictability in the editing process

Despite being highly precise, CRISPR-Cas gene editing can result in off-target effects, where unintended genetic modifications occur at sites other than the intended target. This lack of predictability in the editing process raises concerns about the safety and potential unintended consequences of using CRISPR technology in therapeutic applications. Regulatory bodies and investors may be cautious in supporting applications until these concerns are addressed. Genetic systems are complex, and making even small changes can have unforeseen downstream effects. In both research and therapeutic contexts, there is a risk that CRISPR-Cas gene editing could inadvertently cause changes that impact the organism's health or behavior. This unpredictability can lead to hesitancy in moving forward with applications. The long-term consequences of gene editing are not always well understood. The lack of predictability in terms of how edited genes will behave over time, particularly in the context of human therapies, can raise concerns about introducing genetic changes that might have unintended health implications down the line. Regulatory agencies often require thorough assessments of the potential risks and uncertainties associated with new technologies. The lack of predictability in CRISPR-Cas gene editing outcomes can lead to longer and more stringent regulatory processes, potentially delaying the commercialization of CRISPR-based products. The lack of predictability in outcomes can lead to challenges in designing and executing clinical trials. Uncertainty regarding safety and efficacy outcomes can slow down trial recruitment and approval processes. The unpredictable nature of gene editing outcomes might undermine public confidence in the technology's safety and effectiveness. This, in turn, can affect investor willingness to support research and commercialization efforts in the CRISPR and Cas genes market. The lack of predictability can prompt researchers to exercise caution and demand rigorous studies to validate the outcomes of gene editing experiments. While this is important for scientific integrity, it might slow down the pace of research and development.

Key Market Trends

Growing demand for CRISPR-Based Diagnostics

CRISPR-based diagnostics leverage the precision of CRISPR-Cas gene editing to detect specific genetic sequences associated with diseases, pathogens, or genetic mutations. These diagnostics offer rapid and accurate detection of targets, leading to early and precise disease identification. CRISPR-based diagnostics have the potential to be developed as point-of-care tests, allowing healthcare providers to perform tests at the patient's location rather than sending samples to centralized labs. This convenience and speed are especially beneficial for infectious disease detection and monitoring. CRISPR-based diagnostics can rapidly identify pathogens such as viruses and bacteria in clinical samples. They have the potential to revolutionize infectious disease management by enabling timely interventions, such as isolation and treatment, to control outbreaks. CRISPR-based diagnostics can identify genetic mutations associated with various types of cancer. This early detection can lead to better treatment outcomes by allowing for personalized therapies tailored to a patient's specific genetic profile. CRISPR-based diagnostics can screen for genetic mutations linked to inherited disorders. This can enable early identification of at-risk individuals, facilitating timely interventions and family planning decisions. The adoption of CRISPR-based diagnostics has the potential to drive market growth by expanding the range of applications for CRISPR-Cas technology beyond traditional gene editing. This diversification can attract new players and investments to the CRISPR market.

Growing Synthetic Biology Applications

Synthetic biology involves engineering biological systems for new functions or enhanced performance. CRISPR-Cas technology is a crucial tool in synthetic biology, enabling precise modifications to genes, pathways, and regulatory elements. The demand for advanced gene editing tools drives the growth of the CRISPR and Cas genes market. Synthetic biology applications often require the creation of custom microorganisms with specific genetic traits. CRISPR-Cas technology allows researchers to efficiently engineer microorganisms for purposes such as biofuel production, bioremediation, and industrial enzyme production. The ability to edit genes using CRISPR-Cas systems plays a pivotal role in optimizing biomanufacturing processes. This includes modifying microorganisms to produce valuable pharmaceuticals, chemicals, and other industrial products efficiently. Synthetic biology techniques, coupled with CRISPR-Cas technology, can be used to design and engineer therapeutic molecules, such as antibodies and enzymes, for treating diseases. This intersection of synthetic biology and CRISPR has implications for personalized medicine and drug development. Researchers in synthetic biology aim to design and create organisms with tailored traits. CRISPR-Cas technology facilitates the customization of organisms' genetic makeup to achieve desired characteristics, from improved agricultural traits to enhanced bioproduction capabilities. The synergy between synthetic biology and CRISPR-Cas technology creates new opportunities for innovation and commercialization. Startups and established biotech companies can leverage these tools to develop novel products and solutions for various industries. The combination of CRISPR-Cas technology and synthetic biology provides valuable tools for educational and research purposes. Students and scientists can gain hands-on experience in genetic engineering and explore the potential applications of these technologies.

Segmental Insights

Product & Service Insights

Based on the product & service, the product segment is anticipated to witness substantial market growth throughout the forecast period. This growth can be attributed to multiple factors, such as Several cutting-edge technologies, such as CRISPR gene editing kits, have been developed to meet the growing demands for genome editing solutions. The increased market share is due to the availability of enhanced individual products that can be used to achieve a variety of goals, including simple gene knockouts, selective genome cleavage, reduced off-target cutting, genome engineering, and higher specificity. CRISPR services provide customized gene editing solutions for researchers and companies. Service providers offer expertise in designing guide RNAs, performing gene knockouts, introducing specific mutations, and more. Outsourcing gene editing services to specialized providers allows researchers and companies to access advanced techniques and expertise without investing in establishing in-house capabilities. The convenience and technical support offered by service providers contribute to market growth.

End-use Insights

Based on the end-use segment, the pharmaceutical and biotechnology companies’ segment has been the dominant force in the market. Biotech and pharmaceutical companies invest heavily in R&D to advance CRISPR-Cas technology and its applications. They conduct in-depth studies to improve the efficiency, specificity, and safety of gene editing techniques. They contribute to the development of new CRISPR-based products, services, and therapies, expanding the market's offerings and driving innovation. These companies are actively working on developing CRISPR-based therapies for treating genetic disorders, cancer, and other diseases. Their expertise in drug development, clinical trials, and regulatory pathways accelerates the translation of CRISPR technology into viable treatments. Collaborations between biotech/pharmaceutical companies and academic research institutions enhance the development and commercialization of CRISPR-based products. Such partnerships leverage expertise, resources, and infrastructure to accelerate advancements. Biotech and pharmaceutical companies drive innovation by developing novel CRISPR technologies, methods, and applications. They actively seek intellectual property protection for their inventions, which can shape the competitive landscape of the market.


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Regional Insights

North America, specifically the CRISPR and Cas Genes Market, dominated the market in 2023, primarily due to North America, particularly the United States, boasts a robust research ecosystem with numerous prestigious universities, research institutions, and biotech hubs. These institutions have been at the forefront of CRISPR research, driving technological advancements and innovative applications. Many of the world's leading biotechnology and pharmaceutical companies with significant investments in CRISPR technology are based in North America. These companies have played a pivotal role in advancing CRISPR-based products and therapies. The regulatory landscape in North America, including the United States and Canada, has been relatively supportive of biotechnology and genetic research. This has facilitated research, development, and commercialization of CRISPR-based products, including therapeutic applications. Collaboration between academia, industry, and research institutions in North America has accelerated the development and application of CRISPR technology. This collaborative spirit has resulted in rapid advancements and the expansion of the market.

Recent Developments

  • In February 2023, Ensoma completed the acquisition of Twelve Bio ApS, a company exploring therapeutic applications of next-generation CRISPR-Cas medicines. Such initiatives are expected to boost the market growth in the coming years.

Key Market Players

  • AstraZeneca plc
  • Addgene Inc.
  • Cellectis Bioresearch Inc.
  • CRISPR Therapeutics Inc.
  • Editas Medicine, Inc.
  • F. Hoffmann-La Roche Ltd.
  • Horizon Discovery Group plc
  • Editas Medicine, Inc.
  • GenScript Corp.
  • Merck KGaA.

By Product & Service

By Application

By End-use

By Region

  • Product
  • Service
  • Biomedical
  • Agricultural  
  • Biotechnology & Pharmaceutical Companies
  • Academic & Government Research Institutes
  • Contract Research Organizations (CROs)
  • North America
  • Europe
  • Asia Pacific
  • South America
  • Middle East & Africa
 

Report Scope:

In this report, the Global CRISPR and Cas Genes Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

  • CRISPR and Cas Genes Market, By Product & Service:

o   Product

o   Service

  • CRISPR and Cas Genes Market, By Application:

o   Biomedical

o   Agricultural

  • CRISPR and Cas Genes Market, By End-use:

o   Biotechnology & Pharmaceutical Companies

o   Academic & Government Research Institutes

o   Contract Research Organizations (CROs)

  • CRISPR and Cas Genes Market, By Region:

o   North America

§  United States

§  Canada

§  Mexico

o   Europe

§  France

§  United Kingdom

§  Italy

§  Germany

§  Spain

o   Asia-Pacific

§  China

§  India

§  Japan

§  Australia

§  South Korea

o   South America

§  Brazil

§  Argentina

§  Colombia

o   Middle East & Africa

§  South Africa

§  Saudi Arabia

§  UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global CRISPR and Cas Genes Market.

Available Customizations:

Global CRISPR and Cas Genes market report with the given market data, Tech Sci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

  • Detailed analysis and profiling of additional market players (up to five).

Global CRISPR and Cas Genes Market is an upcoming report to be released soon. If you wish an early delivery of this report or want to confirm the date of release, please contact us at [email protected]

Table of content

1.    Product Overview

1.1.  Market Definition

1.2.  Scope of the Market

1.2.1.    Markets Covered

1.2.2.    Years Considered for Study

1.2.3.    Key Market Segmentations

2.    Research Methodology

2.1.  Objective of the Study

2.2.  Baseline Methodology

2.3.  Key Industry Partners

2.4.  Major Association and Secondary Sources

2.5.  Forecasting Methodology

2.6.  Data Triangulation & Validation

2.7.  Assumptions and Limitations

3.    Executive Summary

3.1.  Overview of the Market

3.2.  Overview of Key Market Segmentations

3.3.  Overview of Key Market Players

3.4.  Overview of Key Regions/Countries

3.5.  Overview of Market Drivers, Challenges, Trends

4.    Voice of Customer

5.    Global CRISPR and Cas Genes Market Outlook

5.1.  Market Size & Forecast

5.1.1.    By Value

5.2.  Market Share & Forecast

5.2.1.    By Product & Service (Product and Service)

5.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

5.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

5.2.2.    By Application (Biomedical, Agricultural)

5.2.3.    By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

5.2.4.    By Region

5.2.5.    By Company (2023)

5.3.  Market Map

6.    North America CRISPR and Cas Genes Market Outlook

6.1.  Market Size & Forecast    

6.1.1.    By Value

6.2.  Market Share & Forecast

6.2.1.    By Product & Service (Product and Service)

6.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

6.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

6.2.2.    By Application (Biomedical, Agricultural)

6.2.3.    By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

6.2.4.    By Country

6.3.  North America: Country Analysis

6.3.1.    United States CRISPR and Cas Genes Market Outlook

6.3.1.1.        Market Size & Forecast

6.3.1.1.1.           By Value

6.3.1.2.        Market Share & Forecast

6.3.1.2.1.           By Product & Service

6.3.1.2.2.           By Application

6.3.1.2.3.           By End-use

6.3.2.    Canada CRISPR and Cas Genes Market Outlook

6.3.2.1.        Market Size & Forecast

6.3.2.1.1.           By Value

6.3.2.2.        Market Share & Forecast

6.3.2.2.1.           By Product & Service

6.3.2.2.2.           By Application

6.3.2.2.3.           By End-use

6.3.3.    Mexico CRISPR and Cas Genes Market Outlook

6.3.3.1.        Market Size & Forecast

6.3.3.1.1.           By Value

6.3.3.2.        Market Share & Forecast

6.3.3.2.1.           By Product & Service

6.3.3.2.2.           By Application

6.3.3.2.3.           By End-use

7.    Europe CRISPR and Cas Genes Market Outlook

7.1.  Market Size & Forecast    

7.1.1.    By Value

7.2.  Market Share & Forecast

7.2.1.    By Product & Service (Product and Service)

7.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

7.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

7.2.2.    By Application (Biomedical, Agricultural)

7.2.3.    By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

7.2.4.    By Country

7.3.  Europe: Country Analysis

7.3.1.    France CRISPR and Cas Genes Market Outlook

7.3.1.1.        Market Size & Forecast

7.3.1.1.1.           By Value

7.3.1.2.        Market Share & Forecast

7.3.1.2.1.           By Product & Service

7.3.1.2.2.           By Application

7.3.1.2.3.           By End-use

7.3.2.    Germany CRISPR and CAS GENES MARKET OUTLOOK

7.3.2.1.        Market Size & Forecast

7.3.2.1.1.           By Value

7.3.2.2.        Market Share & Forecast

7.3.2.2.1.           By Product & Service

7.3.2.2.2.           By Application

7.3.2.2.3.           By End-use

7.3.3.    United Kingdom CRISPR AND Cas Genes Market Outlook

7.3.3.1.        Market Size & Forecast

7.3.3.1.1.           By Value

7.3.3.2.        Market Share & Forecast

7.3.3.2.1.           By Product & Service

7.3.3.2.2.           By Application

7.3.3.2.3.           By End-use

7.3.4.    Italy CRISPR and Cas Genes Market Outlook

7.3.4.1.        Market Size & Forecast

7.3.4.1.1.           By Value

7.3.4.2.        Market Share & Forecast

7.3.4.2.1.           By Product & Service

7.3.4.2.2.           By Application

7.3.4.2.3.           By End-use

7.3.5.    Spain CRISPR and Cas Genes Market Outlook

7.3.5.1.        Market Size & Forecast

7.3.5.1.1.           By Value

7.3.5.2.        Market Share & Forecast

7.3.5.2.1.           By Product & Service

7.3.5.2.2.           By Application

7.3.5.2.3.           By End-use

8.    Asia-Pacific CRISPR and Cas Genes Market Outlook

8.1.  Market Size & Forecast    

8.1.1.    By Value

8.2.  Market Share & Forecast

8.2.1.    By Product & Service (Product and Service)

8.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

8.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

8.2.2.    By Application (Biomedical, Agricultural)

8.2.3.    By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

8.2.4.    By Country

8.3.  Asia-Pacific: Country Analysis

8.3.1.    China CRISPR and Cas Genes Market Outlook

8.3.1.1.        Market Size & Forecast

8.3.1.1.1.           By Value

8.3.1.2.        Market Share & Forecast

8.3.1.2.1.           By Product & Service

8.3.1.2.2.           By Application

8.3.1.2.3.           By End-use

8.3.2.    India CRISPR and CAS GENES MARKET OUTLOOK

8.3.2.1.        Market Size & Forecast

8.3.2.1.1.           By Value

8.3.2.2.        Market Share & Forecast

8.3.2.2.1.           By Product & Service

8.3.2.2.2.           By Application

8.3.2.2.3.           By End-use

8.3.3.    Japan CRISPR and Cas Genes Market Outlook

8.3.3.1.        Market Size & Forecast

8.3.3.1.1.           By Value

8.3.3.2.        Market Share & Forecast

8.3.3.2.1.           By Product & Service

8.3.3.2.2.           By Application

8.3.3.2.3.           By End-use

8.3.4.    South Korea CRISPR and Cas Genes Market Outlook

8.3.4.1.        Market Size & Forecast

8.3.4.1.1.           By Value

8.3.4.2.        Market Share & Forecast

8.3.4.2.1.           By Product & Service

8.3.4.2.2.           By Application

8.3.4.2.3.           By End-use

8.3.5.    Australia CRISPR and Cas Genes Market Outlook

8.3.5.1.        Market Size & Forecast

8.3.5.1.1.           By Value

8.3.5.2.        Market Share & Forecast

8.3.5.2.1.           By Product & Service

8.3.5.2.2.           By Application

8.3.5.2.3.           By End-use

9.    South America CRISPR and Cas Genes Market Outlook

9.1.  Market Size & Forecast    

9.1.1.    By Value

9.2.  Market Share & Forecast

9.2.1.    By Product & Service (Product and Service)

9.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

9.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

9.2.2.    By Application (Biomedical, Agricultural)

9.2.3.    By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

9.2.4.    By Country

9.3.  South America: Country Analysis

9.3.1.    Brazil CRISPR and Cas Genes Market Outlook

9.3.1.1.        Market Size & Forecast

9.3.1.1.1.           By Value

9.3.1.2.        Market Share & Forecast

9.3.1.2.1.           By Product & Service

9.3.1.2.2.           By Application

9.3.1.2.3.           By End-use

9.3.2.    Argentina CRISPR and Cas Genes Market Outlook

9.3.2.1.        Market Size & Forecast

9.3.2.1.1.           By Value

9.3.2.2.        Market Share & Forecast

9.3.2.2.1.           By Product & Service

9.3.2.2.2.           By Application

9.3.2.2.3.           By End-use

9.3.3.    Colombia CRISPR and Cas Genes Market Outlook

9.3.3.1.        Market Size & Forecast

9.3.3.1.1.           By Value

9.3.3.2.        Market Share & Forecast

9.3.3.2.1.           By Product & Service

9.3.3.2.2.           By Application

9.3.3.2.3.           By End-use

10. Middle East and Africa CRISPR and Cas Genes Market Outlook

10.1.        Market Size & Forecast        

10.1.1. By Value

10.2.        Market Share & Forecast

10.2.1. By Product & Service (Product and Service)

10.2.1.1 By Product (Kits & Enzymes, Libraries, Design Tool, Antibodies, Others)

10.2.1.2 By Service (Cell Line Engineering, gRNA Design, Microbial Gene Editing, DNA Synthesis)

10.2.2. By Application (Biomedical, Agricultural)

10.2.3. By End-use (Biotechnology & Pharmaceutical Companies, Academic & Government Research Institutes, Contract Research Organizations (CROs))

10.2.4. By Country

10.3.        MEA: Country Analysis

10.3.1. South Africa CRISPR and Cas Genes Market Outlook

10.3.1.1.     Market Size & Forecast

10.3.1.1.1.         By Value

10.3.1.2.     Market Share & Forecast

10.3.1.2.1.         By Product & Service

10.3.1.2.2.         By Application

10.3.1.2.3.         By End-use

10.3.2. Saudi Arabia CRISPR and Cas Genes Market Outlook

10.3.2.1.     Market Size & Forecast

10.3.2.1.1.         By Value

10.3.2.2.     Market Share & Forecast

10.3.2.2.1.         By Product & Service

10.3.2.2.2.         By Application

10.3.2.2.3.         By End-use

10.3.3. UAE CRISPR and Cas Genes Market Outlook

10.3.3.1.     Market Size & Forecast

10.3.3.1.1.         By Value

10.3.3.2.     Market Share & Forecast

10.3.3.2.1.         By Product & Service

10.3.3.2.2.         By Application

10.3.3.2.3.         By End-use

11. Market Dynamics

11.1.        Drivers

11.2.        Challenges

12. Market Trends & Developments

12.1.        Recent Development

12.2.        Mergers & Acquisitions

12.3.        Product Launches

13. Global CRISPR and Cas Genes Market: SWOT Analysis

14. Porter’s Five Forces Analysis

14.1.        Competition in the Industry

14.2.        Potential of New Entrants

14.3.        Power of Suppliers

14.4.        Power of Customers

14.5.        Threat of Substitute Products

15. Competitive Landscape

15.1.         AstraZeneca plc

15.1.1. Business Overview

15.1.2. Company Snapshot

15.1.3. Products & Services

15.1.4. Financials (As Reported)

15.1.5. Recent Developments

15.1.6. Key Personnel Details

15.1.7. SWOT Analysis

15.2.         Addgene Inc.

15.3.         Cellectis Bioresearch Inc.

15.4.         CRISPR Therapeutics Inc.

15.5.         Editas Medicine, Inc.

15.6.         F. Hoffmann-La Roche Ltd.

15.7.         Horizon Discovery Group plc

15.8.         Editas Medicine, Inc.

15.9.         GenScript Corp.

15.10.      Merck KGaA.

16.  Strategic Recommendations

17.  About Us & Disclaimer

Figures and Tables

Frequently asked questions

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The market size of the Global CRISPR and Cas Genes Market was estimated to be USD 2.40 Billion in 2023.

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The biotechnology and pharmaceutical companies segment demonstrated significant dominance in 2023, primarily driven by pharmaceutical companies are utilizing these technologies to quickly identify and validate new therapeutic targets and to produce better biological models for human diseases in less time are boosting the market growth.

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North America emerged as the dominant market in 2023, capturing a significant revenue share. Growing biopharmaceutical R&D as well as the involvement of several pharmaceutical corporations in the creation of novel therapeutics are also likely to fuel the market growth.

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Due to the availability of enhanced individual products that can be used to achieve a variety of goals, including simple gene knockouts, selective genome cleavage, reduced off-target cutting, genome engineering, and higher specificity are the major drivers for the Global CRISPR and Cas Genes Market.

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Sakshi Bajaal

Business Consultant
Press Release

CRISPR and Cas Genes Market to Grow at 16.28% CAGR over 2025 to 2029

Feb, 2024

Increasing investment by biotechnology companies for novel therapeutics is expected to drive the Global CRISPR and Cas Genes Market growth in the forecast period, 2025-2029.