Human Fibroblast From Skin-Mental Retardation
The Human skin fibroblasts from a mental retardation donor model provide insights into the neurodevelopmental disorders and metabolic defects.
人源与动物源原代细胞,覆盖神经、内分泌、消化、血液、免疫、呼吸、泌尿、生殖、运动 9 大系统,另含 PBMCs 与其他原代细胞。 共 905 个产品。
The Human skin fibroblasts from a mental retardation donor model provide insights into the neurodevelopmental disorders and metabolic defects.
Human Fibroblast From Skin-Muscular Dystrophy-Dystroglycanopathy, Type B serves as a primary model for extracellular matrix and regenerative research.
Human Fibroblast From Skin-Nemaline Myopathy 2 offers a rare disease model for investigating skeletal muscle pathology and therapeutic target discovery.
Human Fibroblast From Skin-Neuropathy, Hereditary Sensory And Autonomic, Type III provides a patient-derived model for cellular function studies.
Human Fibroblast From Skin-Osteogenesis Imperfecta Type IV offers a disease-relevant in vitro model for skeletal biology and genetic disorder research.
Human Fibroblast From Skin-Rett Syndrome provides a patient-derived model for studying MECP2-related neurodevelopmental disorders and therapeutic testing.
Human Fibroblast From Skin-Schuurs-Hoeijmakers Syndrome provides patient-derived fibroblasts for disease modeling, functional studies, and drug discovery.
Human Fibroblast From Skin-Smith-Magenis Syndrome provides a patient-derived model for genetic disease, neurodevelopmental biology, and drug testing.
The Human Fibroblast From Skin-Spinal Muscular Atrophy, Type II provides a model for studying SMA disease mechanisms and therapeutic screening.
Human Fibroblast From Skin-Tay-Sachs Disease offers a model for lysosomal storage disorders, ganglioside metabolism, and therapeutic studies.
Human Fibroblast From Skin-Trisomy 21 provides a cellular model for Down syndrome research, developmental studies, and therapeutic evaluation in vitro.
Human Fibroblast From Skin-Wieacker-Wolff Syndrome provides a unique model for rare X-linked disorder research, genetic analysis, and disease mechanisms.
Human Fibroblast From Skin-Xeroderma Pigmentosum, High-quality cells for XPV research, DNA repair, UV damage response, and genomic stability studies.
Human Fibroblast-Alagille Syndrome 1: High-quality cell line ideal for studies on ALAGILLE SYNDROME 1, ALGS1.
Human Fibroblast-Canavan Disease enables ASPA deficiency modeling and supports neurodegenerative disease screening and lysosomal enzyme profiling.
Human Fibroblast-Cerebral Creatine Deficiency Syndrome 1 is a patient-derived fibroblast model for metabolic disorder research and therapeutic screening.
Human Fibroblast-Glycogen Storage Disease II provides primary fibroblasts for metabolic disorder studies, enzyme deficiency research, and drug testing.
Human Fibroblast-Leigh Syndrome: High-quality cell line ideal for studies on Leigh Syndrome, LS.
Human Fibroblast-Like Synoviocyte (Embryonic) provide reliable models with high post-thaw viability for joint biology, inflammation, and pathology.
Human Fibroblast-Like Synoviocyte Osteo Arthritis, Adult provides primary synoviocytes from OA patients for joint inflammation and arthritis research.
Human Fibroblast-Like Synoviocyte Rheumatoid Arthritis, Adult supports RA pathogenesis studies, joint inflammation modeling, and drug response profiling.
Human Normal HFLS synthesize ECM and lubricate joints; under RA stimuli, they secrete IL-6 and MMPs, modeling inflammation and pannus formation.
Human Fibroblast-Niemann-Pick Disease model offers insights into lipid storage disorders and potential therapeutic strategies for Niemann-Pick.
Human Fibroblast-Tuberous Sclerosis 2 provides patient-derived fibroblasts for TSC2 disease modeling, mTOR pathway studies, and therapeutic research.
共 905 个产品 | 第 17 / 38 页