本分类收录的细胞产品与配套技术资料，支持按来源、物种与规格筛选。 共 293 个产品。
Order HighQC™ human iPSC-derived dopaminergic neurons (CHCHD2 R145Q, HOM) for Parkinson’s research, QC-backed and ready to culture for in vitro studies.
Leverage HighQC™ Human iPSC-Derived Glutamatergic Neurons-Huntington’s Disease Model for neurodegeneration, enabling enzyme activity and drug discovery.
HighQC™ Human Neural Stem Cells (iPSC-derived, SOD1 mutant, A4V, HOM) express Nestin, Pax6, Sox1 and are ideal for ALS modeling and drug testing.
HighQC™ Human Niemann Pick Type C IPSCs ,Patient-derived NPC1-mutant iPSCs for Niemann-Pick disease pathogenesis and neurodegeneration modeling.
HighQC™ IPSC (KO) LRRK2-/- supports neuronal and glial differentiation for Parkinson’s disease modeling, drug discovery, and neurotoxicity assessment.
HighQC™ IPSC (KO) SOD1-/-, ALS, Biallelic KO provides an isogenic ALS model enabling neuron and glia differentiation, disease mechanisms, and screening.
iPSC (induced Pluripotent Stem cells) reprogrammed from human Fibroblasts of a Gaucher Syndrome (Morbus Gaucher) patient.
HighQC™ iPSC from Fibroblast-TRISOMY 21 supports Down syndrome research with validated pluripotency, stable trisomy 21 karyotype, and Sendai reprogramming.
HighQC™ IPSC from Fibroblast, African American, Male, Neonatal supports developmental biology, disease modeling, and cell therapy applications.
IPSC human Foreskin Fibroblast Passage: 1 500,000 cells This iPS cell line was created using a normal human foreskin fibroblast. The iPS cell line was generated using an episomal reprogramming containing a prprietary mix of vectors, containing Oct-4, Sox-2, Klf-4 along with p53 Anti-sense, EBNA-1. Thus, a newborn foreskin fibroblast was reprogrammed into induced pluripotent stem cells (iPSC). The cell line was validated for pluripotency based on colony morphology, alkaline phosphatase expression, and expression of SSEA-4. iPS colonies exhibit classical morphology and growth. Absence of Mycoplasma was confirmed. The cell line is shipped on dry ice.
HighQC™ KCNK3 Knock-out Human Induced Pluripotent Stem Cells provide an iPSC model for ion channel, electrophysiology, and cardiopulmonary studies.
HighQC™ LLGL1 Knock-out Human iPSC line with homozygous exon 5 deletion supports polarity, neurodevelopment, and disease modeling with confirmed.
HighQC™ LRP1 Knockout Human iPSCs are valuable for studying lipid metabolism and developing gene-editing therapies for cardiovascular research.
Explore ImmunoClone's HighQC™ Monkey iPSC from Bone Marrow CD34+. Elevate your scientific research with our premium, validated stem cell products.
Access HighQC™ Mouse Induced Pluripotent Stem (IPS) Cells-Derived Endothelial Cells for vascular development research and in vitro angiogenesis modeling.
HighQC™ Neural Stem Cell (iPSC From ALS Fibroblasts) from ImmunoClone, a robust model for ALS pathology, neurodegeneration, and therapeutic exploration.
HighQC™ Pancreatic Beta Cells Derived From Human Induced Pluripotent Stem Cell enable diabetes modeling, drug testing, and insulin secretion assays.
HighQC™ PLN Knock-out Human Induced Pluripotent Stem Cells enable cardiac disease modeling and PLN-associated calcium signaling studies in human iPSCs.
Utilize HighQC™ RFP-Expressing Human Induced Pluripotent Stem Cells to visualize reprogramming efficiency and study lineage-specific differentiation.
HighQC™ RFP-Human iPSC-Derived Endothelial Precursor Cells enable vascular lineage tracing, differentiation, and endothelial model development.
Normal human iPSC-derived dopaminergic neurons. Functionally active cells ideal for Parkinson's disease modeling, neurotoxicity, and drug discovery.
The Human iPSC from B-Lymphocyte-Nemaline Myopathy 3 serves as a disease-specific model for skeletal muscle research and regenerative medicine.
Human iPSC From Blood-Cancer of Breast provides a disease-specific pluripotent stem cell model for breast cancer research and drug discovery applications.
Human iPSC From Blood-Central Core Disease of Muscle ,High-quality iPSC line for studying Central Core Disease of Muscle and RYR1 function and pathology.
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