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CRISPR 技术市场:按产品、应用和最终用户划分 - 2024-2030 年全球预测CRISPR Technology Market by Offering (Product, Services), Application (Agricultural, Biomedical, Industrial), End User - Global Forecast 2024-2030 |
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预计2023年CRISPR技术市场规模为32.5亿美元,预计2024年将达到37.7亿美元,2030年将达到94.9亿美元,复合年增长率为16.52%。
成簇规则间隔短回文重复序列 (CRISPR) 是源自细菌防御机制的高度精确且高效的基因组编辑工具,可对生物体基因组内的 DNA 序列进行有针对性的操作。这种创新的生物技术工具能够利用 RNA 引导的 Cas9 核酸酶进行精确的基因组编辑,从而促进医疗保健、农业和生质能源产业的标靶基因修饰。研究活动资金的增加、基因治疗的进步、遗传病患病率的增加以及对更有效率作物生产方法的需求正在推动 CRISPR 技术的使用增加。然而,围绕基因编辑(特别是在人类生殖细胞中)的伦理问题以及各个地区的监管障碍可能会阻碍 CRISPR 产品的采用和商业化。然而,药物发现的进步包括创造具有更高营养价值和抗病虫害能力的新型作物,以及使用 CRISPR 系统针对特定标靶筛检大型化合物库,为 CRISPR 创造了利润丰厚的机会。
主要市场统计 | |
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基准年[2023] | 32.5亿美元 |
预测年份 [2024] | 37.7亿美元 |
预测年份 [2030] | 94.9亿美元 |
复合年增长率(%) | 16.52% |
提供的 CRISPR套件和试剂的使用迅速增加,研究活动和产品改进取得进展
CRISPR 技术中使用的酵素是基因编辑的关键组件,其中 Cas9 是最常用的酵素。这些酵素充当分子剪刀,可以精确切割和修饰 DNA 序列。引导 RNA 对于引导 Cas 酶靶向细胞 DNA 序列中的特定基因组位置非常重要。研究人员可能需要针对特定目标设计的自订gRNA,或者他们可能更喜欢预先设计的涵盖模型生物或细胞株中常见基因目标的文库。 CRISPR套件和试剂产品系列包括质体、Cas9蛋白、sgRNA(单嚮导RNA)、表达载体、同源定向修復(HDR)模板、病毒递送系统(如腺结合病毒(AAV)和慢病毒)以及溶核产品包括基于电穿孔的转染方法,包括转染装置和脂转染试剂。细胞株工程服务利用CRISPR技术修饰细胞以引入或增强特定功能,使研究人员能够研究基因功能并开发标靶治疗。这项服务对于专门从事药物发现、基因治疗和再生医学的生物製药公司和学术机构至关重要。引导 RNA (gRNA) 和载体系统的设计和建构对于 CRISPR 介导的基因编辑实验至关重要。研究人员依靠这些服务来产生高效、特异性的敲除或敲入模型,这对于功能基因组学、标靶检验研究和疾病建模等应用尤其重要。基于 CRISPR 的筛检服务对于识别新药物标靶和阐明生物途径中重要的遗传交互作用至关重要。
扩大CRISPR技术在农业领域的应用
在农业领域,CRISPR 技术为作物改良、抗病虫害以及提高产量提供了解决方案。 CRISPR技术也应用于生物医学研究,如遗传疾病的基因治疗、癌症免疫治疗、感染疾病治疗等。 CRISPR技术的工业应用包括微生物工程、生质燃料、生医材料和环境生物修復。
最终用户:CRISPR技术在生技公司的潜在应用
学术和政府研究机构主要专注于CRISPR技术的基础研究和新应用的开发。他们对 CRISPR 的需求将产生先进的知识和工具,以了解基因编辑背后的机制,针对人类基因组中的特定基因,并找到各种遗传疾病的潜在治疗解决方案。使用 CRISPR 技术的生物技术公司专注于商业性应用的应用研究,例如优化工业、增强工业生物过程或直接向消费者销售基因工程产品。製药公司正在将 CRISPR 技术应用于治疗,特别是针对遗传性疾病、癌症和肥胖等文明病的药物发现和药物开发。
区域洞察
在美国,由于广泛的研究和开发活动、公共和私营部门的大量投资以及生物资讯学的进步,CRISPR 技术市场正在经历显着成长。此外,农业、生物技术、药物发现和治疗等强劲且稳定成长的行业正在推动对 CRISPR 技术的需求。亚太地区拥有不断成长的生物製药产业,该产业正在大力投资基因编辑技术,以促进农业进步和疾病治疗应用。此外,政府对基因组学研究的支持以及与国际组织的战略联盟等因素正在加速该地区的市场成长。由于其完善的製药基础设施和各个组织对基因组编辑研究计划的资助,欧洲经历了可观的成长。此外,中东和非洲子区隔放在 CRISPR 在镰镰状性贫血和 β 地中海贫血等疾病的治疗应用。
FPNV定位矩阵
FPNV定位矩阵对于评估CRISPR技术市场至关重要。我们检视与业务策略和产品满意度相关的关键指标,以对供应商进行全面评估。这种深入的分析使用户能够根据自己的要求做出明智的决策。根据评估,供应商被分为四个成功程度不同的像限:前沿(F)、探路者(P)、利基(N)和重要(V)。
市场占有率分析
市场占有率分析是一种综合工具,可以对 CRISPR 技术市场中供应商的现状进行深入而详细的研究。全面比较和分析供应商在整体收益、基本客群和其他关键指标方面的贡献,以便更好地了解公司的绩效及其在争夺市场占有率时面临的挑战。此外,该分析还提供了对该行业竞争特征的宝贵见解,包括在研究基准年观察到的累积、分散主导地位和合併特征等因素。这种详细程度的提高使供应商能够做出更明智的决策并制定有效的策略,从而在市场上获得竞争优势。
1. 市场渗透率:提供有关主要企业所服务的市场的全面资讯。
2. 市场开拓:我们深入研究利润丰厚的新兴市场,并分析其在成熟细分市场的渗透率。
3. 市场多元化:提供有关新产品发布、开拓地区、最新发展和投资的详细资讯。
4. 竞争评估和情报:对主要企业的市场占有率、策略、产品、认证、监管状况、专利状况和製造能力进行全面评估。
5. 产品开发与创新:提供对未来技术、研发活动和突破性产品开发的见解。
1.CRISPR技术市场的市场规模与预测为何?
2.在CRISPR技术市场的预测期间内,有哪些产品、细分市场、应用和领域需要考虑投资?
3.CRISPR技术市场的技术趋势和法规结构是什么?
4. CRISPR技术市场主要厂商的市场占有率是多少?
5.进入CRISPR技术市场的合适型态和策略手段是什么?
[183 Pages Report] The CRISPR Technology Market size was estimated at USD 3.25 billion in 2023 and expected to reach USD 3.77 billion in 2024, at a CAGR 16.52% to reach USD 9.49 billion by 2030.
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) is a highly precise and efficient genome-editing tool derived from a bacterial defense mechanism, which allows for targeted manipulation of the DNA sequence within an organism's genome. This innovative biotechnology tool enables precise genome editing through RNA-guided Cas9 nucleases, facilitating targeted genetic modifications across healthcare, agriculture, and bioenergy industries. Increased funding for research activities, advancements in gene therapy, the growing prevalence of genetic disorders, and the need for more efficient crop production methods increase the use of CRISPR technology. However, ethical concerns surrounding gene editing, especially in human germline cells, and regulatory hurdles in different regions may impede the adoption or commercialization of CRISPR products. Nevertheless, creating new genetically modified crops (GMO) with enhanced nutritional value or resistance to pests and diseases and advancing drug discovery by screening large libraries of compounds against specific targets using CRISPR systems creates lucrative opportunities for the CRISPR technology market.
KEY MARKET STATISTICS | |
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Base Year [2023] | USD 3.25 billion |
Estimated Year [2024] | USD 3.77 billion |
Forecast Year [2030] | USD 9.49 billion |
CAGR (%) | 16.52% |
Offering: Increasing use of CRISPR kits & reagents with the surging research activities and product improvements
The enzymes used in CRISPR technology are critical components for gene editing, with Cas9 being the most commonly utilized enzyme. These enzymes function as molecular scissors, enabling precise cutting and modification of DNA sequences. Guide RNAs have significance in directing the Cas enzymes to target specific genomic locations within a cell's DNA sequence. Researchers may require custom gRNAs designed for their particular targets or prefer pre-designed libraries that cover common gene targets in model organisms or cell lines. The CRISPR kits & reagent product portfolio comprises a range of products, including plasmids, Cas9 proteins, sgRNAs (single guide RNAs), expression vectors, homology-directed repair (HDR) templates, viral delivery systems such as adeno-associated viruses (AAV) or lentiviruses, electroporation-based transfection methods including nucleofection devices or lipofection reagents. Cell line engineering services involve modifying cells to introduce or enhance specific features using CRISPR technology, enabling researchers to study gene function and develop targeted therapies. This service is crucial for biopharmaceutical companies and academic institutions focused on drug discovery, gene therapy, and regenerative medicine. The design and construction of guide RNAs (gRNAs) and vector systems are essential in CRISPR-mediated gene editing experiments. Researchers rely on these services for generating knockout or knock-in models with high efficiency and specificity, which is particularly important in applications such as functional genomics, target validation studies, and disease modeling. CRISPR-based screening services are pivotal for identifying novel drug targets or uncovering critical genetic interactions within biological pathways.
Application: Proliferating use of CRISPR technology in the agricultural sector
In the agricultural sector, CRISPR technology provides solutions for crop improvement, pest and disease resistance, and increased yield. CRISPR technology has applications in biomedical research, such as gene therapy for genetic disorders, cancer immunotherapy, and infectious disease treatment. The industrial applications of CRISPR technology encompass microbial engineering, biofuels, biomaterials, and environmental bioremediation.
End-User: Potential application of CRISPR technology in biotechnology companies
Academic and government research institutes primarily focus on fundamental research and developing novel applications for CRISPR technology. Their need-based preference for CRISPR revolves around generating advanced knowledge and tools to understand the mechanism behind gene editing, targeting specific genes in the human genome, and finding potential therapeutic solutions for various genetic disorders. Biotechnology companies utilizing CRISPR technology focus on applied research with commercial applications such as agriculture optimization, industrial bioprocessing enhancement, or direct-to-consumer genetic modification products. Pharmaceutical companies involve therapeutic applications of CRISPR technology for drug discovery and development, specifically targeting genetic diseases, cancers, or lifestyle disorders such as obesity.
Regional Insights
In America, the CRISPR technology market represents significant growth due to extensive research and development activities, substantial investments by both public and private sectors, and advances in bioinformatics. In addition, robust and steadily growing sectors such as agriculture, biotechnology, drug discovery, and therapeutics increased demand for CRISPR technology. The APAC region boasts increasing biopharmaceutical industries investing heavily in gene-editing technologies for agricultural advancements and disease treatment applications. Additionally, factors such as government support for genomics research and strategic collaborations with international organizations have accelerated market growth in this region. Europe has experienced considerable growth due to its well-established pharmaceutical infrastructure and funding from various organizations for genome editing research projects. Moreover, the Middle-East and Africa sub-segments focus on therapeutic applications of CRISPR for diseases such as sickle cell anemia and beta-thalassemia.
FPNV Positioning Matrix
The FPNV Positioning Matrix is pivotal in evaluating the CRISPR Technology Market. It offers a comprehensive assessment of vendors, examining key metrics related to Business Strategy and Product Satisfaction. This in-depth analysis empowers users to make well-informed decisions aligned with their requirements. Based on the evaluation, the vendors are then categorized into four distinct quadrants representing varying levels of success: Forefront (F), Pathfinder (P), Niche (N), or Vital (V).
Market Share Analysis
The Market Share Analysis is a comprehensive tool that provides an insightful and in-depth examination of the current state of vendors in the CRISPR Technology Market. By meticulously comparing and analyzing vendor contributions in terms of overall revenue, customer base, and other key metrics, we can offer companies a greater understanding of their performance and the challenges they face when competing for market share. Additionally, this analysis provides valuable insights into the competitive nature of the sector, including factors such as accumulation, fragmentation dominance, and amalgamation traits observed over the base year period studied. With this expanded level of detail, vendors can make more informed decisions and devise effective strategies to gain a competitive edge in the market.
Key Company Profiles
The report delves into recent significant developments in the CRISPR Technology Market, highlighting leading vendors and their innovative profiles. These include Agilent Technologies, Inc., Applied StemCell, Inc., Beam Therapeutics Inc., Caribou Biosciences, Inc., Cellectis S.A., CRISPR Therapeutics AG, Danaher Corporation, Editas Medicine, Inc., ERS Genomics Limited, Function Oncology, GeneCopoeia, Inc., GenScript Biotech Corporation, Horizon Discovery Group Ltd. by Revvity, Inc., Inscripta, Inc., Intellia Therapeutics, Inc., Lonza Group Ltd., Mammoth Biosciences, Inc., Merck KGaA, New England Biolabs, Inc., OriGene Technologies, Inc., Prime Medicine, Inc., Scribe Therapeutics, Sherlock Biosciences, Inc., Synthego Corporation, Takara Holdings Inc., Thermo Fisher Scientific Inc., ToolGen, Inc., TriLink BioTechnologies by Maravai Intermediate Holdings, LLC, Twist Bioscience Corporation, and Verve Therapeutics, Inc..
Market Segmentation & Coverage
1. Market Penetration: It presents comprehensive information on the market provided by key players.
2. Market Development: It delves deep into lucrative emerging markets and analyzes the penetration across mature market segments.
3. Market Diversification: It provides detailed information on new product launches, untapped geographic regions, recent developments, and investments.
4. Competitive Assessment & Intelligence: It conducts an exhaustive assessment of market shares, strategies, products, certifications, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players.
5. Product Development & Innovation: It offers intelligent insights on future technologies, R&D activities, and breakthrough product developments.
1. What is the market size and forecast of the CRISPR Technology Market?
2. Which products, segments, applications, and areas should one consider investing in over the forecast period in the CRISPR Technology Market?
3. What are the technology trends and regulatory frameworks in the CRISPR Technology Market?
4. What is the market share of the leading vendors in the CRISPR Technology Market?
5. Which modes and strategic moves are suitable for entering the CRISPR Technology Market?