CL-0133
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Product Introduction
| Cell Name | KLE |
| Synonyms | CVCL_1329 |
| Cellosaurus Accession | CVCL_1329 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Tissue | Uterus; Endometrium |
| Age | 64Y |
| Sex | Female |
| Instructions | 1. Check all containers for leakage or breakage. 2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation. |
| Complete Medium | DMEM/F12 [PM150312]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:3 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 3-5 min |
| Subculturing Procedure | 1. Remove the culture medium from the T25 cell culture flask. 2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS. 3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask. 4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment. 5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension. 6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant. 7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation. |
| Freeze Medium | Freezing Medium (Serum-free & animal origin-free) [PB180438] |
| Storage Conditions | For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only. |
| Background | KLE cells were derived from the endometrial tumor tissue of a 64-year-old Caucasian female and established in 1984 by G.R. Richardson. KLE cells are aneuploid, with a chromosome number ranging from 51 to 66. Electron microscopy reveals tight intercellular junctions and microvilli on the cell surface following xenograft tumor formation in nude mice. The morphological features of KLE cells are consistent with those of the endometrium under progestational stimulation. |
| Tumorigenic | Yes, Tumors developed within 21 days at 100% frequency (5/5) in nude mice inoculated subcutaneously with 1×10⁷ cells. |
| Antigen Expression | Blood Type O; Rh+ |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Human Cell (2023) IF: 4.3
DOI: 10.1007/s13577-023-00920-8
Product Cited: KLE Cells Line
Journal: OncoTargets and Therapy (2023) IF: 4
DOI: 10.2147/OTT.S426923
Product Cited: Ishikawa Cells Line, HEC-1-B Cells Line, AN3 CA Cells Line, KLE Cells Line, RL95-2 Cells Line
Journal: Bioengineered (2022) IF: 4.9
DOI: 10.1080/21655979.2022.2036912
Product Cited: Human Endometrial Epithelial cells, KLE Cells Line, RL95-2 Cells Line, Ishikawa Cells Line
Journal: OncoTargets and Therapy (2021) IF: 4.4
DOI: 10.2147/OTT.S311792
Product Cited: KLE Cells Line, McCoy's 5A
Journal: Drug Design Development and Therapy (2021) IF: 4.319
DOI: 10.2147/DDDT.S304128
Product Cited: McCoy's 5A Medium, KLE Cells Line, McCoy's 5A
