CL-0277
$ 360.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| Cell Name | HCC 94 [HCC941122] |
| Synonyms | HCC-94;HCC94 |
| Cellosaurus Accession | CVCL_6945 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | cervical cancer cells |
| Tissue | Uterus; Cervix |
| Age | 37Y |
| Sex | Female |
Handling information
| 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 | RPMI-1640 [PM150110]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:3-1:4 |
| 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 | General Freezing Medium [PB180436] |
| 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. |
Reference materials
| Background | HCC 94 [HCC941122] cells were derived from a highly differentiated uterine squamous cell carcinoma. The cell line was established in 1995 from the second-passage tumor tissue of a nude mouse xenograft (HCC 94V), which was derived from a human cervical well-differentiated squamous cell carcinoma. After adherent culture, cell growth initiated on day 6, and the first passage was performed on day 38. HCC 94 [HCC941122] cells can form tumors when subcutaneously transplanted into BALB/c-nu/nu nude mice. |
Documents
Publications
Long Noncoding RNA TOB1-AS1 Represses Cervical Cancer Cell Proliferation, Invasion, and Migration via the MicroRNA-27a-3p/Thioredoxin-Interacting Protein Molecular Axis
Journal: KAOHSIUNG JOURNAL OF MEDICAL SCIENCES (2025) IF: 3.1
DOI: 10.1002/kjm2.70076
Product Cited: SiHa Cells Line, Ca Ski Cells Line, C-33 A Cells Line, HCC 94 Cells Line
Predicting therapeutic drugs for hepatocellular carcinoma based on tissue-specific pathways
Journal: Plos Computational Biology (2021) IF: 4.3
DOI: 10.1371/journal.pcbi.1008696
Product Cited: HCC 94 [HCC941122] Cells Line, Hep G2 Cells Line, Hep 3B2.1-7 Cells Line
Long non-coding RNA ABHD11-AS1 facilitates the progression of cervical cancer by competitively binding to miR-330–5p and upregulating MARK2
Journal: Experimental Cell Research (2021) IF: 3.7
DOI: 10.1016/j.yexcr.2021.112929
Product Cited: HCC 94 [HCC941122] Cells Line
