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Product Code | IM-HBMEC |
Species | Human |
Cat.No | ABC-H0025X |
Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
Product Category | Immortalized Cell Lines |
Size/Quantity | 1 vial |
Cell Type | Endothelial |
Shipping Info | Dry Ice |
Growth Conditions | 37 ℃, 5% CO2 |
Source Organ | Brain |
Disease | Normal |
Biosafety Level | 1 |
Storage | Liquid Nitrogen |
Product Type | Immortalized Cell Line |
Immortalized Human Brain Microvascular Endothelial Cells (IM-HBMEC) are developed by immortalizing primary human brain microvascular endothelial cells (HBMECs) using the SV40 Large T antigen. These cells maintain the immune barrier properties of primary HBMECs. IM-HBMEC cells exhibit a polygonal, cobblestone-like morphology and grow as adherent monolayers. They can undergo more than 30 passages without senescence, unlike primary HBMECs, which undergo early senescence after the 3rd passage.The IM-HBMEC cell line is non-tumorigenic and does not exhibit metastatic behavior. It mimics primary HBMECs in assays such as leukocyte migration, cytokine production, and reactions to astrocyte coculture. Flow cytometry shows no significant differences in immune responses compared to primary HBMECs. The cells express VE-cadherin, ZO-1, and claudin-5, essential for blood-brain barrier integrity.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
Immortalized Human Brain Microvascular Endothelial Cells (IM-HBMEC) offer a cost-effective model for constructing in vitro models of the blood-brain barrier (BBB). These immortalized cells exhibit exceptional fidelity in terms of barrier resistance, immune migration, and cytokine response. With their specialized BBB endothelial phenotype, this newly established human cell line provides a readily available in vitro model for studying the properties of the human BBB. IM-HBMECs are particularly valuable for investigating central nervous system infections, offering a valuable alternative to primary brain endothelial cells as a reliable model for studying the blood-brain barrier in such studies.