A704 cell

SKU:BHC11100081
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Overview
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A704 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 Adenocarcinoma
Morphology Epithelial-like
Growth Properties Monolayer, adherent
Tissue Kidney
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Catalog no. Size
300217 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 300217
Species Human
A-704 is a human epithelial cell line derived from kidney tissue of a 78-year-old male patient with adenocarcinoma. This cell line exhibits an epithelial morphology. It is a valuable resource in cancer research, particularly for studying adenocarcinoma. A-704 is a versatile cell line with applications in 3D cell culture and as a transfection host. Derived by D.J. Giard, A-704 maintains consistency and reliability in experimental settings. Karyotype analysis reveals that A-704 cells exhibit abnormalities such as breaks, dicentrics, and endoreduplication, ranging from diploid to hyperdiploid, hypertriploid to hypertetraploid. While not tumorigenic in immunosuppressed mice, A-704 cells can form colonies in a semisolid medium. A-704 cells exhibit specific isoenzyme profiles, including AK-1, ES-D, G6PD, GLO-I, Me-2, PGM1, and PGM3.

SKU:BHC11100081

  • Isoenzymes: Me-2, 1, PGM3, 1-2, PGM1, 1, ES-D, 1, AK-1, 1, GLO-1, 2, G6PD, B
  • Tumorigenic: No
  • Karyotype: (P59) diploid to hyperdiploid, hypertriploid to hypertetraploid with abnormalities including breaks, dicentrics and endoreduplication
  • 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
  • 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: 2 to 3 times per week
  • postThawRecovery: After thawing, plate the cells at 5 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere 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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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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