Cell Line: SW-626

  • Cell Line: SW-626
  • Synonyms:
    • SW-626
    • SW 626
    • SW626
  • Culture Type: Cell line
  • Keywords:  Human Adenocarcinoma Cell Line
  • Description: Established from the ovaries of a 46-year-old, Caucasian female patient with adenocarcinoma. A recent report suggest that the cell line might have been derived from an ovarian metastasis of a primary adenocarcinoma of the colon
  • Origin:
    • Organism:
      • Species: Human (Homo sapiens)
      • Age: 46 years
      • Ethnicity: Caucasian
      • Gender: Female
    • Tissue: Ovary #
    • Disease: Adenocarcinoma
    • Primary/Metastasis: Metastatic (DepMap)
    • Collection site: Ovary (DepMap)
    • Year of origin: 1974
    • Country of Origin: United States
  • Cell line features:
    • Cell Type: Epithelial
    • Morphology: Epithelial-like
    • Growth mode: Adherent
    • Life span: Infinite (continuous culture)
    • Karyotype: Hypertetraploid, modal number = 104
    • Doubling time:-
    • Microsatellite instability: Stable
    • Special features:-
    • Product:-
    • Soft agar colony formation assay:-
    • Tumorigenicity: tumorigenic in nude mice 
    • Gene expression:-
    • Sequence variations:
      • KRAS (G12V mutation, Oncogenic, Gain-of-function, Heterozygous)
      • TP53 (G262V mutation, Likely Oncogenic, Likely Loss-of-function,  Homozygous)
      • For information, please visit
        • https://depmap.org/portal/cell_line/ACH-001399?tab=mutations
        • https://depmap.org/portal/cell_line/ACH-001399?tab=fusions
  • Handling and maintenance:
    • Biosafety level: BSL 1 (ATCC) (It may differ in your country, follow the guidelines of your institute/country)
    • Complete culture medium:
      • Leibovitz’s L-15 Medium + 10% FBS (ATCC)
    • Culture conditions: 
      • Temperature: 37°C incubator
      • Atmosphere: 100% Air
    • Subculturing:
      • Subculturing method: Enzymatic dissociation
      • Cell dissociation solution: 0.25% (w/v) Trypsin- 0.53 mM EDTA solution
      • Harvesting time: Subconfluent culture (70% confluency) (Cells do not reach confluency but will grow in small islands)
      • Seeding density:-
      • Recommended split ratio: 1:2 to 1:5
      • Medium Renewal: 2 to 3 times per week
    • Cryopreservation:
      • Freezing medium: Complete growth medium + 5% (v/v) DMSO
      • Storage conditions: Vapor phase of liquid nitrogen
      • Cell suspension (cell density):-
      • Volume per vial: 1 ml
  • Applications: 
    • 3D cell culture
    • Cancer research

# A recent report suggest that the cell line might have been derived from an ovarian metastasis of a primary adenocarcinoma of the colon

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