For research use only
| Cat No. | ABC-SC0102T |
| Product Type | Animal Embryonic Stem Cells |
| Cell Type | Fibroblast |
| Species | Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Embryo |
| Disease | inflammatory conditions |
| Storage | Liquid Nitrogen |
Mouse INOS knockout embryonic fibroblasts, isolated from tissue of pathogen-free laboratory mice.
HighQC™ iNOS Knockout Mouse Embryonic Fibroblasts are primary fibroblast cells isolated from embryonic tissues of genetically engineered mice lacking the inducible nitric oxide synthase (iNOS/Nos2) gene. These embryonic fibroblasts are derived from mouse embryos at mid-gestation stages and are classified as primary embryonic somatic cells. Morphologically, they display a typical fibroblast-like phenotype characterized by elongated, spindle-shaped or stellate cells. The cells express the fibroblast marker FSP1/S100A4. Functionally, iNOS-deficient MEFs retain fundamental fibroblast activities including extracellular matrix synthesis, maintenance of stromal architecture, and regulation of intercellular signaling, while exhibiting altered nitric oxide–dependent signaling pathways. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | HighQC™ INOS Knockout Mouse Embryonic Fibroblasts, mEF-iNOS-KO, Mouse Embryonic Fibroblasts iNOS Knockout |
| Species | Mouse |
| Cat.No | ABC-SC0102T |
| Product Category | Stem Cells |
| Size/Quantity | 1 vial |
| Cell Type | Fibroblast |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Embryo |
| Disease | inflammatory conditions |
| Storage | Liquid Nitrogen |
| Product Type | Animal Embryonic Stem Cells |
| Host Cell | Mouse Embryonic Fibroblasts |
HighQC™ iNOS Knockout Mouse Embryonic Fibroblasts (iNOS⁻/⁻ MEFs) provide a genetically defined in vitro model for fundamental studies of nitric oxide–dependent signaling and gene regulation in embryonic fibroblasts. These cells are also suited for mechanistic analyses of transcriptional regulation, epigenetic modulation, and cell cycle control influenced by nitric oxide signaling, as well as for comparative studies with wild-type MEFs to delineate genotype-dependent differences in fibroblast biology under controlled experimental conditions.
When you publish your research, please cite our product as "AcceGen Biotech Cat.# XXX-0000". In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).