AS-30D cell

SKU:BHC11100263
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Overview
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AS-30D cell is a cell line (Female). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Round cells, loosely adherent, floating. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Disease model Hepatocellular carcinoma
Morphology Round cells, loosely adherent, floating
Growth Properties Adherent
Tissue Liver
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Catalog no. Size
500116 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 500116
Species Rat
Established in vitro from the AS-30D tumor ascites.

SKU:BHC11100263

  • Tumorigenic: Yes, in Sprague-Dawley rats
  • Viruses: RAP-test: Negative.
  • Karyotype: Hypodiploid rat karyotype with 12% tetraploidy, 38 (35-41).
  • cultureMedium: RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
  • supplements: Supplement the medium with 10% FBS
  • doublingTime: 26 hours
  • subculturing: Gently homogenize the cell suspension in the flask by pipetting up and down, then take a representative sample to determine the cell density per ml. Dilute the suspension to achieve a cell concentration of 1 x 105 cells/ml with fresh culture medium, and aliquot the adjusted suspension into new flasks for further cultivation.
  • seedingDensity: A seeding density of 1 x 106 cells/ml is recommended.
  • fluidRenewal: Every 3 to 5 days
  • postThawRecovery: After thawing, allow the cells to recover from the freezing process for at least 24 hours.
  • 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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