HNO258 cell

SKU:BHC11100301
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Overview
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HNO258 cell is a cell line derived from Caucasian (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Monolayer, adherent, Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Head and neck squamous cell carcinoma (HNSCC)
Morphology Epithelial-like
Growth Properties Monolayer, adherent
Tissue Oral cavity
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Catalog no. Size
300146 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 300146
Species Human
The HNO258 cell line is derived from an oral squamous cell carcinoma, which is a subtype of head and neck squamous cell carcinoma (HNSCC). This cell line exhibits several chromosomal abnormalities, which have been identified through chromosomal comparative genomic hybridization (cCGH). Specifically, HNO258 has shown DNA copy number gains in the chromosomal regions 1q41, 3q21-qter, 7p, 7cen-q21, 8q22-qter, 9cen-p13, 9q31-qter, 11q13, 15p, and 15q. Additionally, it displays copy number losses in the regions 4p and 18q12-qter. These genetic alterations are common in HNSCC and are associated with tumorigenesis and cancer progression. The amplification of 11q13, observed in HNO258, is particularly noteworthy due to its association with the overexpression of oncogenes such as CCND1 (cyclin D1) and CTTN (cortactin), which are involved in cell cycle regulation and cytoskeletal organization, respectively. These oncogenes are frequently implicated in the aggressive behavior of cancer cells, contributing to increased proliferation and invasiveness. The detailed genetic characterization of HNO258 makes it a valuable model for studying the molecular mechanisms underlying oral squamous cell carcinoma and for evaluating potential therapeutic strategies that target these specific genetic alterations.

SKU:BHC11100301

  • cultureMedium: DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
  • supplements: Supplement the medium with 10% FBS
  • 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.
  • 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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