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Humanized model of the immune system
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iHuPBMC-T
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iHuPBMC-NK
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iHuPBMC-B
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PBMC-LT
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CD34+ HSC
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Winn model
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iHuPBMC-MHC/KO
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iHuPBMC-OncVax
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PBMC mixed inoculation model
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In vivo tumor experimental platform
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CDX
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iHuPDX
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Non-GLP Toxicology
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PK/PD
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Brain in situ model
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Other in situ models
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Hematologic tumor model system inoculation
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Creation of high interstitial tumor models
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In vitro killing experiment platform
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Immune co-culture killing model
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CDC
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In vitro killing experiment platform
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IC50
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PDC High-Throughput In Vitro Pharmacodynamics
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3D organoids
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ADCC
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T cell-mediated killing experiment
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Mouse-derived immune system model
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Tumor vaccine
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Cell therapy
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In vitro testing platform
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Non-GLP Toxicology Platform
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Non-tumor model and drug efficacy evaluation platform
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Systematic Vaccination Model
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Non-tumor model and drug efficacy evaluation platform
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Skin injury model
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Stroke model
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Liver fibrosis model
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Diabetes model
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Gouty Arthritis (GA) Model
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Pulmonary fibrosis model
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Systemic lupus erythematosus (SLE) model
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Inflammatory Bowel Disease (IBD) model
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Rheumatoid Arthritis (RA) Model
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PDX model
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PDX model
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Head and neck cancer
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Eye cancer
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Lung cancer
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Human breast cancer
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Esophageal cancer in humans
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Human gastric cancer
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Colorectal cancer
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Human liver cancer
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Bile duct cancer
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Gallbladder cancer
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Human pancreatic cancer
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Human kidney cancer
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Human Bladder Cancer
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Ureteral cancer
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Prostate cancer
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Uterine cancer
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Cervical cancer in women
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Human Ovarian Cancer
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Human skin cancer
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sarcoma
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Human Nervous System Cancer
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Embryonal carcinoma
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Human Lymphoma
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Human leukemia
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Multiple Myeloma
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Adrenal gland
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Mesothelioma
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Other people
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CDX model
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CDX model
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Head and neck cancer
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Eye cancer
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Lung cancer
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Human breast cancer
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Esophageal cancer in humans
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Human gastric cancer
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Colorectal cancer
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Human liver cancer
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Bile duct cancer
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Gallbladder cancer
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Human pancreatic cancer
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Human kidney cancer
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Human Bladder Cancer
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Ureteral cancer
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Prostate cancer
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Uterine cancer
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Cervical cancer in women
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Human Ovarian Cancer
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Human skin cancer
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sarcoma
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Human Nervous System Cancer
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Embryonal carcinoma
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Human Lymphoma
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Human leukemia
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Multiple Myeloma
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Adrenal gland
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Mesothelioma
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Other people
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Homogeneous Model
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Homogeneous Model
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Head and neck cancer
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Eye cancer
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Lung cancer
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Breast cancer
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Stomach cancer
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Liver cancer
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Bile duct cancer
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Gallbladder cancer
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Pancreatic cancer
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Kidney cancer
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Bladder cancer
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Ureteral cancer
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Prostate cancer
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Uterine cancer
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Cervical cancer
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Ovarian cancer
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Esophageal cancer
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Skin cancer
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sarcoma
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Nervous System Cancer
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Embryonal carcinoma
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Lymphoma
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Leukemia
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Multiple Myeloma
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Adrenal gland
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Mesothelioma
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Other
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Colorectal cancer
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News Center
——
InnoModels Biotechnology:Key Benefits of the InnoModels Humanized Model of the Biological Immune System
Author:
InnoModels
Release time:
2024-04-07
In biomedical research, experimental models that can accurately simulate human physiological mechanisms are essential. The InnoModels Biotechnology Humanized Model of the Immune System (TMIMS) was born to meet this need, and it has shown great potential in the fields of disease research, drug development and immunotherapy with its unique advantages.
First of all, the main advantage of the humanized immune system model is its highly humanized characteristics. Traditional animal models differ greatly from humans in terms of their immune systems, which leads to uncertainty and unpredictability in experimental results. In contrast, the humanized model of immune system of InnoModels Biotechnology introduces key components of the human immune system into the animal model through gene editing and cell transplantation, making the whole model closer to humans in terms of immune response, composition of immune cells, and the development of immune-related diseases.

Secondly, the model provides a more realistic experimental environment for disease research. Since the model has a humanized immune system, researchers can study various immune-related diseases, such as autoimmune diseases, infectious diseases and tumors, under conditions closer to human physiology. This not only contributes to a deeper understanding of the pathogenesis of diseases, but also provides more precise strategies and methods for disease prevention and treatment.
In addition, humanized models of the immune system have shown unique advantages in drug screening and immunotherapy. By simulating the response of the human immune system, the model can more accurately predict the efficacy and side effects of drugs in the human body, thus accelerating the drug development process. At the same time, the model can also be used to evaluate the effectiveness of immunotherapy strategies, providing strong support for personalized treatment and precision medicine.
Last but not least, the humanized model of the immune system is highly flexible and controllable. Researchers can simulate immune system responses in different disease states by adjusting factors such as gene expression, cellular composition and immune stimulation in the model. This flexibility allows researchers to customize personalized experimental models to better meet different research needs.
In summary, InnoModels' humanized model of the immune system provides a powerful tool for biomedical research with its highly humanized properties, realistic experimental environment, potential for drug screening and immunotherapy, and flexibility and controllability. With the continuous progress of technology and the expansion of application fields, we have reason to believe that such models will play an even more important role in the future and make greater contributions to human health.
InnoModels Biotechnology (Beijing) Co., Ltd.
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TEL: +86 15711355061
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E-mail: xuyl@imodels.tech
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Address: Building 14, No. 79 West Shuangying Road, Changping District, Beijing
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