시장보고서
상품코드
1987305

재조합 단백질 시장 규모, 점유율, 동향 및 예측 : 제품별, 용도별, 최종사용자별, 지역별(2026-2034년)

Recombinant Protein Market Size, Share, Trends and Forecast by Product, Application, End User, and Region, 2026-2034

발행일: | 리서치사: 구분자 IMARC | 페이지 정보: 영문 146 Pages | 배송안내 : 2-3일 (영업일 기준)

    
    
    




※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

2025년 세계의 재조합 단백질 시장 규모는 23억 달러로 평가되었습니다. IMARC Group은 2026-2034년 CAGR 9.17%로 성장을 지속하여 2034년에는 시장 규모가 50억 4,000만 달러에 달할 것으로 예측했습니다. 현재 북미가 시장을 주도하고 있으며, 2025년에는 40%의 시장 점유율을 차지했습니다. 이 지역은 탄탄한 바이오 의약품 인프라, 주요 학술 연구센터의 집중, 생명과학 부문에 대한 막대한 정부 자금 지원, 임상 및 치료 현장에서의 적극적인 바이오 의약품 채택 등의 이점을 누리고 있으며, 이 모든 것이 결합되어 재조합 단백질 시장 점유율을 확대하고 있습니다.

이 시장은 주로 만성질환 및 희귀질환의 전 세계 유병률 증가로 인해 고급 치료 솔루션에 대한 수요가 증가하고 있습니다. 제약사 및 바이오 제약사들이 저분자 치료제에서 재조합 단백질과 같은 바이오 의약품에 집중하는 추세는 다양한 치료 영역에서 엄청난 성장 기회를 가져다주고 있습니다. 전 세계 정부 기관들의 단백질체학 및 유전체학 연구에 대한 투자 확대는 진단 및 치료를 위한 혁신적인 재조합 단백질 기반 솔루션의 개발을 촉진하고 있습니다. 첨단 재조합 단백질 발현 플랫폼의 개발은 면역 치료 절차에 널리 사용되는 고품질 자가 항원 개발을 가속화하는 데 일조하고 있습니다. 또한, 분자생물학, 단백질체학, 세포생물학에서 연구 시약으로 재조합 단백질의 사용이 증가하고 있으며, 그 응용 범위가 넓어지고 있습니다. 특히 특허가 만료된 생물학적 제제를 대상으로 한 바이오시밀러 개발에 대한 관심이 높아지면서 세계 생명과학 산업에서 재조합 단백질의 혁신과 대규모 생산에 대한 시장 전망이 밝아지고 있습니다.

미국은 여러 요인으로 인해 재조합 단백질 시장의 주요 지역으로 부상하고 있습니다. 미국에는 연구 대학, 전문 바이오테크놀러지 클러스터, 국립보건원(NIH) 등의 기관이 연방정부의 강력한 지원을 바탕으로 세계에서 가장 발전된 바이오의약품 생태계를 보유하고 있습니다. 성숙한 벤처 캐피탈 환경은 초기 단계의 재조합 단백질 치료제에 대한 지속적인 자금 조달을 가능하게 하고, 기초 연구부터 상업적 생산에 이르는 파이프라인을 가속화하고 있습니다. 미국의 규제 환경은 생물학적 제제 및 바이오시밀러 승인에 사용되는 체계적인 프로세스를 제공하여 혁신적인 재조합 단백질 제품 시장 진입을 가속화함으로써 재조합 단백질 시장의 성장을 뒷받침하고 있습니다. 미국 식품의약국(FDA) 데이터에 따르면, 2024년에는 50개의 새로운 치료제가 승인될 것으로 예상되며, 그 중 16개는 단백질 기반 치료제로 전체 승인 건수의 32%를 차지할 것으로 예측됩니다. 이러한 견조한 승인 실적은 바이오의약품 혁신 분야에서 미국의 리더십과 여러 치료 분야에 걸친 재조합 단백질 시장 예측 가능한 솔루션에 대한 지속적인 수요를 반영합니다.

재조합 단백질 시장 동향

확대되는 항체 기반 치료제 파이프라인

항체 기반 치료제의 개발은 세계 재조합 단백질 시장을 형성하는 가장 혁신적인 트렌드 중 하나로 부상하고 있습니다. 고도의 포유류 및 미생물 세포 시스템을 통해 발현되는 재조합 항체는 뛰어난 표적 특이성, 효능, 잘 밝혀진 안전성 프로파일로 인해 현대 종양학, 면역학 및 희귀질환 치료의 초석이 되고 있습니다. 단일클론항체, 이중 특이성 항체, 항체-약물 복합체(ADC) 파이프라인이 확대되면서 연구 및 상업적 생산 부문에서 고품질 재조합 항체 단백질에 대한 지속적인 수요가 발생하고 있습니다. 제약 및 바이오 제약 기업들은 단백질 공학 기술을 활용하여 결합 친화성 향상, 면역원성 감소, 치료 반감기 연장을 위해 차세대 항체 형태에 많은 투자를 하고 있습니다. 또한, 재조합 항체 생산은 질병 관련 바이오마커를 정확하게 식별할 수 있기 때문에 신약 개발 초기 단계의 표적 검증에 점점 더 많이 활용되고 있습니다. 2025년 혈장 유래 의약품을 제조하는 스페인 헬스케어 기업 그리폴스(Grifols)는 네덜란드의 바이오테크 스타트업 FcR Therapeutics와 제휴하여 자가면역질환 치료를 위한 재조합 나노체를 개발한다고 발표했습니다. 개발한다고 발표했습니다.

단백질 공학 및 발현에서 AI의 통합

인공지능과 단백질 공학의 융합은 바이오 의약품 및 연구 부문의 재조합 단백질 생산 워크플로우를 근본적으로 변화시키고 있습니다. 머신러닝 알고리즘과 딥러닝을 통한 단백질 구조 예측 모델과 같은 고급 계산 도구를 통해 연구자들은 안정성, 생물학적 활성, 생산성을 향상시킨 새로운 단백질 변이체를 개발 기간을 대폭 단축하여 설계할 수 있게 되었습니다. 이러한 혁신은 재조합 치료제의 임상 적용 기간을 직접적으로 단축하고, 미생물 및 포유류 발현 시스템에서 생산 수율을 향상시키며, 기존에 구조적으로 복잡했던 단백질 타겟을 개발할 수 있게 해줍니다. 동시에 자동화와 고성능 스크리닝을 단백질 생산 플랫폼에 통합함으로써 최적의 발현 조건을 보다 효율적으로 파악할 수 있어 확장 가능하고 비용 효율적인 생산에 기여하고 있습니다. 규제 당국과 정부 기관은 이러한 기술의 중요성을 인식하고 있으며, 미국 국방부는 '분산형 바이오 산업 제조 프로그램(DBIMP)'을 통해 바이오 산업 기업에 12개의 보조금을 추가로 지원한다고 밝혔습니다. 이번 발표로 DBIMP의 보조금 지원 건수는 현재까지 25건, 총 4,200만 달러에 달하며, 재조합 단백질 시장 전망에 있어 AI를 활용한 플랫폼의 보급이 더욱 가속화될 것으로 예측됩니다.

바이오의약품 연구개발에 대한 정부 투자 증가

바이오의약품 연구개발에 대한 정부의 투자 확대는 세계 시장에서 재조합 단백질 시장의 성장을 견인하는 결정적인 요인으로 부상하고 있습니다. 각국 정부 및 공공 자금 지원 기관은 재조합 단백질을 공중 보건, 경제 경쟁, 바이오 보안을 위해 전략적으로 중요한 자산으로 인식하고 있으며, 개발 및 생산을 촉진하기 위한 전용 프로그램을 수립하고 있습니다. 여러 지역에 걸친 자금 지원 이니셔티브는 단백질 과학의 초기 단계 학술 연구부터 상업적 규모의 바이오 의약품 제조 인프라 개발까지 다양한 활동을 지원하고 있습니다. 이러한 투자는 정부기관, 학계, 민간 바이오 기업 간의 협력을 촉진하고, 치료용 단백질 발견 속도를 가속화할 수 있는 혁신 생태계를 구축하고 있습니다. 국내 생물학적 제제 생산 능력을 확대하기 위한 프로그램은 최근 세계 보건 위기 동안 드러난 공급망 취약성을 완화하고 있습니다. 예를 들어, 인도는 바이오의약품 및 바이오시밀러 개발을 촉진하기 위해 11억 달러 규모의 투자 이니셔티브를 발표했으며, 재조합 단백질 의약품을 우선 치료제로 명시적으로 포함시킴으로써 세계 재조합 단백질 시장 동향을 주도하는 공공 자금의 중요한 역할을 강화하고 있습니다.

목차

제1장 서문

제2장 조사 범위와 조사 방법

제3장 주요 요약

제4장 서론

제5장 세계의 재조합 단백질 시장

제6장 시장 분석 : 제품별

제7장 시장 분석 : 용도별

제8장 시장 분석 : 최종사용자별

제9장 시장 분석 : 지역별

제10장 SWOT 분석

제11장 밸류체인 분석

제12장 Porter의 Five Forces 분석

제13장 가격 분석

제14장 경쟁 구도

LSH 26.04.14

The global recombinant protein market size was valued at USD 2.3 Billion in 2025. Looking forward, IMARC Group estimates the market to reach USD 5.04 Billion by 2034, exhibiting a CAGR of 9.17% from 2026-2034. North America currently dominates the market, holding a market share of 40% in 2025. The region benefits from its robust biopharmaceutical infrastructure, high concentration of leading academic research centers, significant government funding directed toward life sciences, and strong adoption of biologics in clinical and therapeutic settings, all collectively expanding the recombinant protein market share.

The market is being mainly driven by the increasing global incidence of chronic and rare diseases, thus increasing the demand for advanced therapeutic solutions. The increasing trend of pharmaceutical and biopharmaceutical companies shifting their focus from small molecule therapies to biologics, such as recombinant proteins, has opened up immense opportunities for growth in various therapeutic areas. The increasing investment by government organizations across the globe in proteomics and genomics research is helping in the development of innovative recombinant protein-based solutions for diagnosis and treatment. The development of advanced recombinant protein expression platforms has helped in accelerating the development of high-quality autoantigens, which are largely used in immunotherapy procedures. In addition, the increasing use of recombinant proteins as research reagents in molecular biology, proteomics, and cell biology is increasing the applications of recombinant proteins. The increasing interest in the development of biosimilars, especially for off-patent biologic therapeutics, is helping in creating a favorable market outlook for innovation and large-scale manufacturing of recombinant proteins in the global life sciences industry.

The United States has emerged as a major region in the Recombinant Protein market owing to many factors. The country is home to one of the world's most advanced biopharmaceutical ecosystems, supported by a dense network of research universities, specialized biotechnology clusters, and robust federal funding from agencies such as the National Institutes of Health. A mature venture capital environment enables continuous financing of early-stage recombinant protein therapeutics, accelerating the pipeline from laboratory research to commercial production. The regulatory environment in the United States provides structured pathways for the approval of biologics and biosimilars, supporting expedited market entry for innovative recombinant protein products, thereby supporting the recombinant protein market growth. According to data from the U.S. Food and Drug Administration, 50 new therapeutics were approved in 2024, with 16 being protein-based therapies, representing 32% of all approvals. This strong regulatory output reflects the country's leadership in biopharmaceutical innovation and the sustained demand for recombinant protein market forecast solutions across multiple therapeutic areas.

RECOMBINANT PROTEIN MARKET TRENDS:

Expanding Antibody-Based Therapeutic Pipelines

The development of antibody-based therapeutics has emerged as one of the most transformative trends shaping the global recombinant protein market. Recombinant antibodies, expressed through sophisticated mammalian and microbial cell systems, have become the cornerstone of modern oncology, immunology, and rare disease therapies due to their exceptional target specificity, potency, and well-characterized safety profiles. The expanding pipeline of monoclonal antibodies, bispecific antibodies, and antibody-drug conjugates has generated sustained demand for high-quality recombinant antibody proteins across both research and commercial manufacturing settings. Pharmaceutical and biopharmaceutical organizations are channeling considerable investments into next-generation antibody formats, leveraging protein engineering technologies to enhance binding affinity, reduce immunogenicity, and extend therapeutic half-lives. Recombinant antibody production is also being increasingly integrated into early-stage drug target validation, enabling precise identification of disease-associated biomarkers. In 2025, Spain's Grifols, a healthcare firm that produces plasma-derived medicines, revealed a partnership with the Netherlands' FcR Therapeutics, a biotech startup, to create recombinant nanobodies for autoimmune disease treatments.

AI Integration in Protein Engineering and Expression

The convergence of artificial intelligence with protein engineering is fundamentally reshaping recombinant protein production workflows across the biopharmaceutical and research sectors. Advanced computational tools, including machine learning algorithms and deep learning-based protein structure prediction models, are enabling researchers to design novel protein variants with enhanced stability, bioactivity, and manufacturability in considerably shorter development timelines. These innovations are directly reducing the time-to-clinic for recombinant therapeutics, improving production yields in microbial and mammalian expression systems, and enabling the development of previously structurally complex protein targets. Simultaneously, the integration of automation and high-throughput screening into protein production platforms is allowing more efficient identification of optimal expression conditions, contributing to scalable and cost-effective manufacturing. Regulatory agencies and government bodies are recognizing the importance of these technologies, with the United States Department of Defense revealed 12 more grants to bioindustrial companies through the Distributed Bioindustrial Manufacturing Program (DBIMP). This announcement elevates the DBIMP to 25 awards thus far, amounting to $42 million, anticipated to accelerate further adoption of AI-enabled platforms across the recombinant protein market outlook.

Rising Government Investments in Biopharmaceutical R&D

Heightened government investment in biopharmaceutical research and development is emerging as a defining driver of recombinant protein market forecast expansion across global markets. National governments and public funding bodies are increasingly recognizing recombinant proteins as strategically important assets for public health, economic competitiveness, and biosecurity, leading to the establishment of dedicated programs to advance their development and production. Funding initiatives spanning multiple geographies are supporting a range of activities, from early-stage academic research in protein science to commercial-scale biopharmaceutical manufacturing infrastructure development. These investments are catalyzing collaborations between government agencies, academic institutions, and private-sector biotechnology firms, creating innovation ecosystems that accelerate the pace of therapeutic protein discovery. Programs designed to expand domestic biologics production capacities are also reducing supply chain vulnerabilities identified during recent global health disruptions. India, for example, announced a USD 1.1 billion investment initiative to boost the development of biologics and biosimilars, explicitly including recombinant protein drugs among the prioritized modalities, reinforcing the significant role of public funding in driving recombinant protein market trends globally.

RECOMBINANT PROTEIN INDUSTRY SEGMENTATION:

Analysis by Product:

  • Antibodies
  • Hormones
  • Growth Factors
  • Cytokines
  • Others

Antibodies hold 26% of the market share. Recombinant antibodies represent the most widely utilized product category within the recombinant protein market, reflecting their central role in therapeutic development, diagnostic assay design, and biomedical research. These proteins are produced using recombinant DNA technology to achieve high specificity, reproducibility, and batch-to-batch consistency, which are critical attributes for both clinical and laboratory applications. Recombinant antibodies are deployed extensively in immunotherapy regimens targeting cancer, autoimmune disorders, and inflammatory conditions, making them indispensable components of the modern biopharmaceutical pipeline. The segment benefits from rapid advancement of antibody engineering platforms, which have enabled the development of novel antibody formats including bispecific antibodies and antibody-drug conjugates that offer improved therapeutic precision. Moreover, governments are approving new therapeutics, demonstrating significant regulatory momentum behind antibody-based recombinant proteins and their expanding presence in global drug approval pipelines.

Analysis by Application:

  • Drug Discovery and Development
  • Academic Research
  • Biotechnology Research
  • Biopharmaceutical Production
  • Others

Drug discovery and development lead the market with a share of 50%. This segment's commanding position reflects the indispensable role of recombinant proteins in identifying new therapeutic targets, validating drug candidates, and supporting the transition from preclinical models to clinical evaluation. Recombinant proteins serve as essential reagents and biological tools across multiple stages of the drug discovery process, including target identification, lead compound screening, structural biology studies, and preclinical efficacy assessment. The growing pipeline of biologic drugs, driven by the rising prevalence of cancer, diabetes, autoimmune disorders, and rare diseases, has significantly expanded the demand for highly specialized recombinant proteins in drug development workflows. Research organizations and biopharmaceutical companies are heavily investing in protein-based screening platforms that enable rapid and cost-effective evaluation of therapeutic candidates.

Analysis by End User:

  • Pharmaceutical and Biopharmaceutical Companies
  • Biotechnology Companies
  • Academic and Research Institutes
  • Contract Research Organization
  • Others

Pharmaceutical and biopharmaceutical companies dominate the market, with a share of 61%. This segment's leading position stems from the large-scale and multifaceted use of recombinant proteins throughout the drug discovery, development, and commercial manufacturing continuum. Pharmaceutical and biopharmaceutical organizations rely on recombinant proteins as critical research tools for biomarker identification, target validation, and lead optimization, as well as key inputs in the production of biologics including monoclonal antibodies, therapeutic enzymes, and hormones. The ongoing transition from traditional small-molecule drugs to biologic therapies has intensified demand for recombinant protein products, encouraging organizations to expand internal research capabilities and establish partnerships with contract research and manufacturing organizations. Increasing regulatory approvals for novel biologics across major markets are expected to further consolidate the dominance of this segment globally.

Regional Analysis:

  • North America
    • United States
    • Canada
  • Asia Pacific
    • China
    • Japan
    • India
    • South Korea
    • Australia
    • Indonesia
    • Others
  • Europe
    • Germany
    • France
    • United Kingdom
    • Italy
    • Spain
    • Russia
    • Others
  • Latin America
    • Brazil
    • Mexico
    • Others
  • Middle East and Africa

North America, accounting for 40% of the share, enjoys the leading position in the market. The region's dominance is attributable to its highly developed biopharmaceutical industry ecosystem, which encompasses a dense concentration of leading research universities, technology transfer offices, and specialized biotechnology firms engaged in recombinant protein development and manufacturing. Government agencies in North America have consistently allocated substantial funding to life sciences research, creating a stable and innovation-supportive environment for the advancement of recombinant protein technologies. The region also benefits from a mature venture capital ecosystem that enables continuous financing of early-stage therapeutic protein programs, accelerating the journey from discovery to market entry. Well-established regulatory frameworks provide structured pathways for biologics and biosimilar approvals, enabling consistent throughput of recombinant protein-derived products.

KEY REGIONAL TAKEAWAYS:

UNITED STATES RECOMBINANT PROTEIN MARKET ANALYSIS

The United States has established itself as the primary growth engine of the global recombinant protein market, reflecting a powerful convergence of advanced biotechnology infrastructure, robust research and development investments, and a highly favorable regulatory environment. The country hosts a substantial concentration of pharmaceutical and biopharmaceutical companies, academic medical centers, and contract research organizations, each contributing to the continuous expansion of the recombinant protein development pipeline. Federal agencies including the National Institutes of Health and the Department of Defense have maintained substantial funding commitments to biomedical research and biomanufacturing capacity, creating a sustained innovation ecosystem that supports both foundational science and commercial development. The adoption of personalized medicine principles, alongside the rapid expansion of the biosimilar market following multiple biologic patent expirations, is driving additional demand for recombinant protein products. The country's large and aging population, coupled with increasing incidence rates of chronic conditions such as cancer, diabetes, and autoimmune disorders, further strengthens the long-term demand environment. In 2025, Novavax, Inc. announced that the U.S. Food and Drug Administration has granted approval for the Nuvaxovid(TM) 2025-2026 Formula to prevent COVID-19 in individuals aged 65 and older, or those between 12 and 64 with at least one underlying condition that increases their risk for severe COVID-19 outcomes.

EUROPE RECOMBINANT PROTEIN MARKET ANALYSIS

Europe represents the second-largest regional market for recombinant proteins, underpinned by a robust biopharmaceutical ecosystem characterized by strong academic-industry collaborations and a steadily expanding base of biosimilar development activities. Countries such as Germany, France, and the United Kingdom host world-class research institutions and pharmaceutical manufacturers that generate consistent demand for high-purity recombinant proteins across therapeutic research and commercial production stages. The European Medicines Agency provides a well-structured regulatory framework that facilitates the approval of biologics, creating transparent and efficient market entry pathways for recombinant protein-based products. The aging population across key European nations is driving elevated demand for protein-based therapeutics addressing oncology, metabolic diseases, and immunological conditions. Supportive regulatory frameworks are being actively reinforced by new policy initiatives like the European Commission adopted a landmark proposal on December 16, 2025 for the European Biotech Act, a regulatory framework specifically designed to strengthen the Union's biotechnology and biomanufacturing sectors and accelerate the development and commercialization of biologics, including recombinant proteins, across member states.

ASIA-PACIFIC RECOMBINANT PROTEIN MARKET ANALYSIS

Asia-Pacific is emerging as one of the fastest-growing regions in the global recombinant protein market, driven by expanding biopharmaceutical manufacturing capacities, rising incidence of chronic diseases, and supportive government initiatives aimed at building domestic biotechnology capabilities. Countries including China, Japan, India, and South Korea are making significant strides in recombinant protein research, production, and commercialization, fueled by government funding programs and increasing foreign direct investments in biotech infrastructure. The region benefits from growing demand for biosimilars and biologics from rapidly expanding healthcare systems across diverse economies. India demonstrated particularly strong policy commitment to this sector, with the government announcing investment program to boost the development of biologics and biosimilars, explicitly including recombinant protein drugs among prioritized product categories, underscoring its strategic focus on building a globally competitive biopharmaceutical manufacturing base.

LATIN AMERICA RECOMBINANT PROTEIN MARKET ANALYSIS

Latin America is demonstrating increasing potential as a growing market for recombinant proteins, driven by rising healthcare expenditures, expanding biopharmaceutical production capabilities, and the growing burden of chronic diseases such as cancer, diabetes, and cardiovascular conditions. Brazil and Mexico represent the region's largest markets, leveraging investments in healthcare infrastructure and growing biotechnology sectors to expand the domestic production of biologics. Government initiatives across the region are supporting the adoption of biosimilars and recombinant protein-based therapeutics to improve treatment access and reduce healthcare costs.

MIDDLE EAST AND AFRICA RECOMBINANT PROTEIN MARKET ANALYSIS

The Middle East and Africa region represents an emerging market for recombinant proteins, characterized by increasing government investments in healthcare infrastructure, growing pharmaceutical manufacturing capabilities, and the rising prevalence of chronic diseases including diabetes, cancer, and cardiovascular conditions. Gulf Cooperation Council countries, particularly Saudi Arabia and the United Arab Emirates, have been at the forefront of healthcare modernization initiatives, creating expanding opportunities for biopharmaceutical products including recombinant proteins. Saudi Arabia's Vision 2030 initiative has catalyzed substantial investment in healthcare and biotechnology infrastructure, with the kingdom directing considerable resources toward life sciences research and biomanufacturing capabilities.

COMPETITIVE LANDSCAPE:

The global recombinant protein market is characterized by a moderately fragmented competitive landscape, with established multinationals and specialized niche providers actively competing across research-grade, clinical-grade, and commercial-grade recombinant protein segments. Market leaders are deploying diverse growth strategies, including product portfolio expansion, strategic licensing agreements, academic-industry collaborations, and investments in advanced expression system technologies, to maintain and strengthen their competitive positions. The integration of artificial intelligence into protein design and bioprocess optimization is increasingly being leveraged by leading players to differentiate their offerings and deliver faster innovation cycles. Contract development and manufacturing organizations are playing an increasingly important role in the ecosystem, enabling smaller biopharmaceutical companies to access recombinant protein production capabilities without significant capital investment. Mergers, acquisitions, and strategic partnerships between reagent providers, contract manufacturers, and biopharmaceutical developers are reshaping industry boundaries, while regulatory compliance and quality assurance remain critical differentiators as demand from clinical-stage drug developers and commercial manufacturers continues to intensify across major global markets.

The report provides a comprehensive analysis of the competitive landscape in the recombinant protein market with detailed profiles of all major companies, including:

  • Abcam Limited
  • ACROBiosystems
  • Bio-RAD Laboratories Inc.
  • Bio-Techne
  • Bps Bioscience Inc.
  • Enzo Biochem Inc.
  • Genscript
  • Prospec-Tany Technogene Ltd
  • R&D Systems, Inc.
  • RayBiotech, Inc.
  • Sino Biological, Inc
  • Thermo Fisher Scientific Inc

KEY QUESTIONS ANSWERED IN THIS REPORT

1. How big is the recombinant protein market?

2. What is the future outlook of the recombinant protein market?

3. What are the key factors driving the recombinant protein market?

4. Which region accounts for the largest recombinant protein market share?

5. Which are the leading companies in the global recombinant protein market?

Table of Contents

1 Preface

2 Scope and Methodology

  • 2.1 Objectives of the Study
  • 2.2 Stakeholders
  • 2.3 Data Sources
    • 2.3.1 Primary Sources
    • 2.3.2 Secondary Sources
  • 2.4 Market Estimation
    • 2.4.1 Bottom-Up Approach
    • 2.4.2 Top-Down Approach
  • 2.5 Forecasting Methodology

3 Executive Summary

4 Introduction

  • 4.1 Overview
  • 4.2 Key Industry Trends

5 Global Recombinant Protein Market

  • 5.1 Market Overview
  • 5.2 Market Performance
  • 5.3 Impact of COVID-19
  • 5.4 Market Forecast

6 Market Breakup by Product

  • 6.1 Antibodies
    • 6.1.1 Market Trends
    • 6.1.2 Market Forecast
  • 6.2 Hormones
    • 6.2.1 Market Trends
    • 6.2.2 Market Forecast
  • 6.3 Growth Factors
    • 6.3.1 Market Trends
    • 6.3.2 Market Forecast
  • 6.4 Cytokines
    • 6.4.1 Market Trends
    • 6.4.2 Market Forecast
  • 6.5 Others
    • 6.5.1 Market Trends
    • 6.5.2 Market Forecast

7 Market Breakup by Application

  • 7.1 Drug Discovery and Development
    • 7.1.1 Market Trends
    • 7.1.2 Market Forecast
  • 7.2 Academic Research
    • 7.2.1 Market Trends
    • 7.2.2 Market Forecast
  • 7.3 Biotechnology Research
    • 7.3.1 Market Trends
    • 7.3.2 Market Forecast
  • 7.4 Biopharmaceutical Production
    • 7.4.1 Market Trends
    • 7.4.2 Market Forecast
  • 7.5 Others
    • 7.5.1 Market Trends
    • 7.5.2 Market Forecast

8 Market Breakup by End User

  • 8.1 Pharmaceutical and Biopharmaceutical Companies
    • 8.1.1 Market Trends
    • 8.1.2 Market Forecast
  • 8.2 Biotechnology Companies
    • 8.2.1 Market Trends
    • 8.2.2 Market Forecast
  • 8.3 Academic and Research Institutes
    • 8.3.1 Market Trends
    • 8.3.2 Market Forecast
  • 8.4 Contract Research Organization
    • 8.4.1 Market Trends
    • 8.4.2 Market Forecast
  • 8.5 Others
    • 8.5.1 Market Trends
    • 8.5.2 Market Forecast

9 Market Breakup by Region

  • 9.1 North America
    • 9.1.1 United States
      • 9.1.1.1 Market Trends
      • 9.1.1.2 Market Forecast
    • 9.1.2 Canada
      • 9.1.2.1 Market Trends
      • 9.1.2.2 Market Forecast
  • 9.2 Asia-Pacific
    • 9.2.1 China
      • 9.2.1.1 Market Trends
      • 9.2.1.2 Market Forecast
    • 9.2.2 Japan
      • 9.2.2.1 Market Trends
      • 9.2.2.2 Market Forecast
    • 9.2.3 India
      • 9.2.3.1 Market Trends
      • 9.2.3.2 Market Forecast
    • 9.2.4 South Korea
      • 9.2.4.1 Market Trends
      • 9.2.4.2 Market Forecast
    • 9.2.5 Australia
      • 9.2.5.1 Market Trends
      • 9.2.5.2 Market Forecast
    • 9.2.6 Indonesia
      • 9.2.6.1 Market Trends
      • 9.2.6.2 Market Forecast
    • 9.2.7 Others
      • 9.2.7.1 Market Trends
      • 9.2.7.2 Market Forecast
  • 9.3 Europe
    • 9.3.1 Germany
      • 9.3.1.1 Market Trends
      • 9.3.1.2 Market Forecast
    • 9.3.2 France
      • 9.3.2.1 Market Trends
      • 9.3.2.2 Market Forecast
    • 9.3.3 United Kingdom
      • 9.3.3.1 Market Trends
      • 9.3.3.2 Market Forecast
    • 9.3.4 Italy
      • 9.3.4.1 Market Trends
      • 9.3.4.2 Market Forecast
    • 9.3.5 Spain
      • 9.3.5.1 Market Trends
      • 9.3.5.2 Market Forecast
    • 9.3.6 Russia
      • 9.3.6.1 Market Trends
      • 9.3.6.2 Market Forecast
    • 9.3.7 Others
      • 9.3.7.1 Market Trends
      • 9.3.7.2 Market Forecast
  • 9.4 Latin America
    • 9.4.1 Brazil
      • 9.4.1.1 Market Trends
      • 9.4.1.2 Market Forecast
    • 9.4.2 Mexico
      • 9.4.2.1 Market Trends
      • 9.4.2.2 Market Forecast
    • 9.4.3 Others
      • 9.4.3.1 Market Trends
      • 9.4.3.2 Market Forecast
  • 9.5 Middle East and Africa
    • 9.5.1 Market Trends
    • 9.5.2 Market Breakup by Country
    • 9.5.3 Market Forecast

10 SWOT Analysis

  • 10.1 Overview
  • 10.2 Strengths
  • 10.3 Weaknesses
  • 10.4 Opportunities
  • 10.5 Threats

11 Value Chain Analysis

12 Porters Five Forces Analysis

  • 12.1 Overview
  • 12.2 Bargaining Power of Buyers
  • 12.3 Bargaining Power of Suppliers
  • 12.4 Degree of Competition
  • 12.5 Threat of New Entrants
  • 12.6 Threat of Substitutes

13 Price Analysis

14 Competitive Landscape

  • 14.1 Market Structure
  • 14.2 Key Players
  • 14.3 Profiles of Key Players
    • 14.3.1 Abcam Limited
      • 14.3.1.1 Company Overview
      • 14.3.1.2 Product Portfolio
      • 14.3.1.3 Financials
      • 14.3.1.4 SWOT Analysis
    • 14.3.2 ACROBiosystems
      • 14.3.2.1 Company Overview
      • 14.3.2.2 Product Portfolio
      • 14.3.2.3 Financials
      • 14.3.2.4 SWOT Analysis
    • 14.3.3 Bio-RAD Laboratories Inc.
      • 14.3.3.1 Company Overview
      • 14.3.3.2 Product Portfolio
      • 14.3.3.3 Financials
      • 14.3.3.4 SWOT Analysis
    • 14.3.4 Bio-Techne
      • 14.3.4.1 Company Overview
      • 14.3.4.2 Product Portfolio
      • 14.3.4.3 Financials
    • 14.3.5 Bps Bioscience Inc.
      • 14.3.5.1 Company Overview
      • 14.3.5.2 Product Portfolio
    • 14.3.6 Enzo Biochem Inc.
      • 14.3.6.1 Company Overview
      • 14.3.6.2 Product Portfolio
      • 14.3.6.3 Financials
      • 14.3.6.4 SWOT Analysis
    • 14.3.7 Genscript
      • 14.3.7.1 Company Overview
      • 14.3.7.2 Product Portfolio
    • 14.3.8 Prospec-Tany Technogene Ltd
      • 14.3.8.1 Company Overview
      • 14.3.8.2 Product Portfolio
    • 14.3.9 R&D Systems, Inc.
      • 14.3.9.1 Company Overview
      • 14.3.9.2 Product Portfolio
      • 14.3.9.3 Financials
      • 14.3.9.4 SWOT Analysis
    • 14.3.10 RayBiotech, Inc.
      • 14.3.10.1 Company Overview
      • 14.3.10.2 Product Portfolio
      • 14.3.10.3 Financials
      • 14.3.10.4 SWOT Analysis
    • 14.3.11 Sino Biological, Inc
      • 14.3.11.1 Company Overview
      • 14.3.11.2 Product Portfolio
      • 14.3.11.3 Financials
      • 14.3.11.4 SWOT Analysis
    • 14.3.12 Thermo Fisher Scientific Inc
      • 14.3.12.1 Company Overview
      • 14.3.12.2 Product Portfolio
      • 14.3.12.3 Financials
      • 14.3.12.4 SWOT Analysis
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