RLE-6TN cell

SKU:BHC11101680
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Overview
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RLE-6TN cell is a cell line (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Epithelial. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Morphology Epithelial
Growth Properties Adherent
Tissue Lung
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Catalog no. Size
305350 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 305350
Species Rat
The RLE-6TN cell line is an immortalized rat alveolar type II epithelial cell line derived from adult Fischer 344 rats. RLE-6TN was established through spontaneous immortalization during attempts to introduce the SV40-T antigen gene into primary alveolar type II epithelial cells. Unlike its counterpart RLE-6T, which was positively transfected with the SV40-T antigen, RLE-6TN cells do not express the T-antigen gene. Despite this, RLE-6TN cells retain critical morphological and functional features characteristic of alveolar type II cells, including cytokeratin expression and the presence of lipid-containing lamellar inclusion bodies. RLE-6TN cells have been widely used as an in vitro model for investigating lung epithelial cell biology, alveolar function, and responses to various physiological and pathological stimuli. They are particularly relevant for studying Na-K-ATPase regulation and activity in alveolar epithelial cells. Na-K-ATPase is essential for maintaining cellular ion gradients and trans-epithelial ion transport, processes critical for alveolar fluid clearance in the lungs. In studies, thyroid hormone (T3) has been shown to stimulate Na-K-ATPase activity in RLE-6TN cells by enhancing its translocation to the plasma membrane rather than increasing its transcription, highlighting a novel, rapid regulatory mechanism. RLE-6TN cells demonstrate stable growth, with near-diploid karyotype stability, and are not tumorigenic in nude mice. They are negative for alkaline phosphatase activity but stain positive for cytokeratins 8, 18, and 19, confirming their epithelial origin. RLE-6TN cells can be maintained long-term in culture and serve as a reliable platform for mechanistic studies on alveolar epithelial repair, surfactant metabolism, and cellular responses to lung injury, toxins, and therapeutic agents.

SKU:BHC11101680

  • Antigen expression: cytokeratin 8; cytokeratin 19
  • Tumorigenic: No, No not tumorgenic in nude mice
  • Viruses: SV40
  • Karyotype: Cells are reported to remain near diploid and karyotypically stable from passage 19-70 with 50% or more of the cells containing 42 chromosomes. At passage 37, there was a translocation between chromosome 1 and 15 which results in trisomy of the q arm of chromosome 1.
  • cultureMedium: DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a)
  • supplements: Supplement the medium with 5% FBS
  • dissociationReagent: Accutase
  • fluidRenewal: 2 to 3 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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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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