A498 cell

SKU:BHC11100167
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Overview
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A498 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 Renal cell carcinoma
Morphology Epithelial-like
Growth Properties Monolayer, adherent
Tissue Kidney
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Catalog no. Size
300113 1 cryovial
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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 300113
Species Human
A498 cells are a human renal cell carcinoma cell line derived from the kidney tissue of a 58-year-old Caucasian male. These cells are extensively used in research related to kidney cancer, particularly for studying clear cell renal cell carcinoma, which is the most common type of kidney cancer in adults. The A498 cell line is characterized by its epithelial-like morphology and has been a valuable model for investigating the molecular and cellular mechanisms of renal carcinogenesis. These cells exhibit several features typical of kidney cancer, including alterations in the expression of genes involved in cell cycle regulation, apoptosis, and angiogenesis. A498 cells are particularly useful for examining the metabolic pathways altered in kidney cancer, as they display a distinct metabolic profile that includes changes in lipid and glucose metabolism. This aspect makes them suitable for metabolic targeting studies, which explore how altering metabolic pathways can inhibit tumor growth. Furthermore, A498 cells are employed in drug discovery and toxicology studies to test the efficacy of new chemotherapeutic agents and targeted therapies. They are also used to study the response of renal cancer cells to hypoxic conditions-a common feature of solid tumors that significantly influences tumor behavior and treatment response. Overall, the A498 cell line serves as an essential tool in renal cancer research, facilitating the development of more effective therapeutic strategies and enhancing our understanding of kidney cancer biology.

SKU:BHC11100167

  • Isoenzymes: PGM3, 1, PGM1, 1-2, ES-D, 2, Me-2, 1, AK-1, 1, GLO-1, 2, G6PD, B
  • Tumorigenic: Yes, in nude mice. Forms undifferentiated carcinoma, also forms tumors in anti thymocyte serum treated newborn mice
  • MSI status: Stable (MSS)
  • cultureMedium: EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a)
  • supplements: Supplement the medium with 10% FBS and 1% NEAA
  • dissociationReagent: Accutase
  • doublingTime: 62 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 will result in a confluent monolayer within 4 days.
  • fluidRenewal: Every 3 days
  • postThawRecovery: After thawing, plate the cells at 2 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere for at least 24 to 48 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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