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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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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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New Drug Development Services
ADCC
Antibody-dependent cellular cytotoxicity (ADCC)
NK cells play a key role in the natural immune response, responsible for attacking cells marked by antibodies, such as tumor cells.ADCCIn the mechanism, antibodies bind to tumor cell antigens and interact with the activating Fc receptors of NK cells, triggering their cytotoxic activity.
Target cell selection
• Tumor cell lines: Suitable for a wide range of research and testing needs.
• Primary tumor cells: More accurately simulates the biological environment.
• Genetically engineered cell lines: Customized through genetic technology to meet specific research needs.
Source of effector cells
• Commercially sourced PBMCs: Standardized and suitable for most studies.
• PBMCs from clinical patients: More targeted, suitable for specific scenarios.
• NK92 cell line: Specifically designed for NK cell research.
Analysis and detection
• Flow cytometry detection: High precision in distinguishing effective target cells, providing accurate data for research.
• Apoptosis ratio: Using flow cytometry technology to accurately calculate the ratio of apoptotic cells, intuitively assessing the effect of ADCC.
Summary
Our ADCC platform provides you with comprehensive research tools, whether selecting the appropriate cell source or conducting precise analysis and detection, to meet your needs. Explore the potential role of ADCC in tumor therapy, starting from here.
Validate the in vitro ADCC efficacy of Rituximab on Raji cells (effector cells are NK92)
Chuangmo Biotechnology (Beijing) Co., Ltd.
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Telephone:+8615010000264 +8613810723384
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E-mail:cndw@imodels.tech
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Address: Building 14, Life Valley, Shuangying West Road, Changping District, Beijing
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Chuangmo Biotechnology (Beijing) Co., Ltd