SCC-4 cell

SKU:BHC11101507
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Overview
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SCC-4 cell is a cell line derived from Caucasian (Male). 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 Human
Disease model Squamous cell carcinoma
Morphology Epithelial-like
Growth Properties Adherent
Tissue Tongue
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Catalog no. Size
305384 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 305384
Species Human
SCC-4 is a human tongue squamous cell carcinoma (SCC) cell line widely used in cancer research to explore mechanisms of oral cancer progression, apoptosis, and response to chemotherapeutic agents. Oral squamous cell carcinoma is a common malignancy in the oral cavity and is often linked to lifestyle factors such as tobacco use and alcohol consumption. SCC-4 cells are characterized by their aggressive nature and are used to model tumor behavior and treatment resistance in vitro. Studies using SCC-4 have shown that several compounds, such as rhein, emodin, and berberine, induce apoptosis through both intrinsic (mitochondria-dependent) and extrinsic (death receptor-mediated) pathways. Rhein induces S-phase cell cycle arrest and apoptosis through endoplasmic reticulum stress, ROS generation, and mitochondrial dysfunction, triggering the activation of caspase-8, -9, and -3. Similarly, emodin was shown to cause G2/M-phase arrest and induce apoptosis by disrupting mitochondrial membrane potential and promoting cytochrome c release. Berberine also induces apoptosis in SCC-4 cells by enhancing ROS production, increasing intracellular Ca2+, and decreasing mitochondrial membrane potential, thereby activating caspase-9 and caspase-3 pathways. These findings demonstrate that SCC-4 is an effective model for studying the molecular mechanisms of apoptosis in response to potential anticancer agents, providing insight into therapeutic strategies targeting oral squamous cell carcinoma.

SKU:BHC11101507

Mutational profile: Mutation: TP53, p.Pro151Ser (c.451C>T)

  • 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 10% FBS and 400 ng/mL hydrocortisone
  • 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.
  • 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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