CL-0100
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Product Introduction
| Cell Name | HEC-1-B |
| Synonyms | Hec-1-B;HEC-1B;HEC1-B;HEC1B;Hec1B |
| Cellosaurus Accession | CVCL_0294 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Tissue | Uterus; Endometrium |
| Age | 71Y |
| 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 | MEM, with NEAA [PM150410]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:4 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 2-3 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 | HEC-1-B cells are a substrain of HEC-1-A cells, isolated by H. Kuramoto in 1968. In contrast to HEC-1-A cells, HEC-1-B cells exhibit a stationary growth phase between days 135 and 190 in culture. Upon recovery, they appear flattened and display a more pavement-like morphology relative to the parental cell line. Furthermore, the modal chromosome complement of HEC-1-B cells is double that of the parental cell line. |
| Tumorigenic | Yes, in nude mice (The cells form moderately well differentiated adenocarcinomas consistent with endometrial carcinoma (grade II)). Yes, in the cheek pouch of cortisone treated hamsters (The cells form typical papillary adenomas). |
| Antigen Expression | Blood Type B; Rh+ |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: CANCER SCIENCE (2026) IF: 4.3
DOI: 10.1111/cas.70324
Product Cited: Ishikawa Cells Line, THP-1 Cells Line, HEC-1-B Cells Line
Journal: ONCOLOGY RESEARCH (2026) IF: 4.1
Product Cited: AN3 CA Cells Line, HEC-1-B Cells Line, MEM, with NEAA
Journal: TISSUE & CELL (2026) IF: 2.5
DOI: 10.1016/j.tice.2026.103359
Product Cited: DMEM (High glucose) Medium, Ishikawa Cells Line, MEM Medium, HEC-1-B Cells Line, Human Endometrial Stromal Cells, DMEM/F12 Medium, RL95-2 Cells Line
Journal: Taiwanese Journal of Obstetrics & Gynecology (2026) IF: 2.2
DOI: 10.1016/j.tjog.2025.09.025
Product Cited: HEC-1-B Cells Line
Journal: International Journal of Clinical and Experimental Pathology (2026) IF: 0.9
DOI: 10.62347/LSIP9900
Product Cited: HEC-1-B Cells Line
