SaOS-2 cell

SKU:BHC11100434
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Overview
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SaOS-2 cell is a cell line derived from Caucasian (Female). 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 Osteosarcoma
Morphology Epithelial-like
Growth Properties Monolayer, adherent
Tissue Bone
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Catalog no. Size
300331 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 300331
Species Human
Saos-2 cells are an osteosarcoma cell line derived from the primary osteogenic sarcoma of an 11-year-old Caucasian female. These cells are a widely recognized model for studying osteosarcoma and bone biology, due to their osteoblastic characteristics and the ability to produce a bone-like extracellular matrix. Characterized by their high level of alkaline phosphatase activity and expression of bone-specific proteins such as osteocalcin and osteopontin, Saos-2 cells serve as an effective in vitro system to study bone formation and the pathophysiology of osteosarcoma. They are particularly valuable for investigating cellular responses to various biochemical stimuli and mechanical forces that mimic the bone environment. Saos-2 cells also exhibit an aneuploid karyotype, lacking several chromosomes but with extra copies of others, typical of many cancer cell lines. They are negative for mycoplasma and possess a robust capacity for calcification, making them suitable for assays related to mineral deposition. In the context of cancer research, Saos-2 cells are extensively used to explore the molecular mechanisms of tumorigenesis, metastasis, and the effects of anticancer drugs on osteosarcoma. The cells are also employed to study gene expression profiles associated with osteoblastic differentiation and malignancy. Due to their high transfectability, Saos-2 cells are amenable to genetic manipulation, which allows for the study of gene function and the validation of molecular targets for therapeutic intervention. This adaptability has facilitated significant advancements in understanding the genetic and molecular basis of bone cancer and in developing targeted treatments for osteosarcoma.

SKU:BHC11100434

  • Receptors expressed: Epidermal growth factor (EGF), transforming growth factor beta (type 1 and type 2)
  • Antigen expression: Blood Type B, Rh+, HLA A2, A3, Bw16, Bw47
  • Isoenzymes: Me-2, 1, PGM3, 1-2, PGM1, 1-2, ES-D, 2, AK-1, 1, GLO-1, 2, G6PD, B, Phenotype Frequency Product: 0.0002
  • Tumorigenic: No
  • MSI status: Stable (MSS)
  • Karyotype: The stemline chromosome number is hypotriploid with the modal number of 56 chromosomes per cell and the 2S component occurring at 13.2%. Over two-thirds of the chromosome complement consisted of structurally rearranged chromosomes. Most marker chromosomes had complex rearrangements. The origin of the segments composing these markers could not be identified. Of the identifiable markers, 6p+/q+, 7p+, 11p+, and 12p+ occasionally were present at 2 copies per cell. The Y chromosome was not detected in the QM stained preparation.
  • 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
  • dissociationReagent: Accutase
  • doublingTime: 35 to 40 hours
  • 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.
  • seedingDensity: 1 x 104 cells/cm2
  • fluidRenewal: 2 to 3 times per week
  • postThawRecovery: Fast
  • 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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