IEC-18 cell

SKU:BHC11101575
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Overview
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IEC-18 cell is a Epithelial cell cell line (Unspecified). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Disease model Normal
Morphology Epithelial-like
Growth Properties Adherent
Tissue Small intestine, ileum
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Catalog no. Size
305302 1 cryovial
Available Options

This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Mfr No 305302
Species Rat
The IEC-18 cell line is a non-transformed epithelial cell line derived from the crypt cells of rat small intestine. These cells have been shown to effectively model the physiological properties of the small intestinal epithelium, particularly with respect to chloride ion (Cl⁻) transport. Chloride channels in IEC-18 cells exhibit distinct types of conductances that respond to various stimuli such as cell swelling, increased intracellular calcium (Ca²⁺), and elevated cyclic AMP (cAMP). For instance, swelling-activated Cl⁻ currents in IEC-18 cells are characterized by outward rectification and voltage independence. Moreover, IEC-18 cells express cystic fibrosis transmembrane conductance regulator (CFTR) channels, evidenced by the presence of cAMP-activated Cl⁻ conductance which can be inhibited by glibenclamide and 5-nitro-2-(3-phenylpropylamino) benzoic acid (NPPB), but not affected by DIDS. IEC-18 cells have also been used to explore cell survival mechanisms under detachment-induced stress, known as anoikis. Research indicates that prostaglandin E2 (PGE2) can promote cell viability and aggregation in detached IEC-18 cells through cAMP-mediated signaling pathways. This protection from anoikis is associated with the activation of adenylate cyclase and protein kinase A (PKA), enhancing cell adhesion and viability even in suspended states. Such findings are significant for understanding inflammation-related processes and potential contributions to carcinogenesis in intestinal tissues. Furthermore, IEC-18 monolayers have been employed to study the transport of various molecules across the intestinal barrier. Compared to the Caco-2 cell line, IEC-18 cells provide a more accurate model for passive transcellular and paracellular transport due to their structural similarities to small intestine crypt cells. Unlike Caco-2 cells, which possess significant active transport capabilities, IEC-18 cells demonstrate minimal carrier-mediated transport, making them a more suitable choice for analyzing the passive permeability of hydrophilic macromolecules.

SKU:BHC11101575

  • cultureMedium: DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
  • supplements: Supplement the medium with 10% FBS
  • dissociationReagent: Accutase
  • subculturing: Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
  • seedingDensity: 2 x 104 cells/cm2
  • fluidRenewal: 2 times per week
  • freezeMedium: As a cryopreservation medium, use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
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