JAR cell

SKU:BHC11100379
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Overview
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JAR cell is a cell line derived from Caucasian (Female). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Choriocarcinoma
Morphology Epithelial-like
Growth Properties Adherent
Tissue Placenta
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Catalog no. Size
300221 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
Species Human
The JAR cell line is a human choriocarcinoma cell line derived from trophoblastic cells of placental origin. This cell line is widely utilized in cancer research, particularly in studies related to gestational trophoblastic diseases and placental development. JAR cells exhibit characteristics typical of choriocarcinoma, including high levels of human chorionic gonadotropin (hCG) production, which makes them a valuable model for studying hormone regulation, placental biology, and the mechanisms underlying trophoblastic tumorigenesis. JAR cells are known for their invasive properties and ability to proliferate rapidly, which mirrors the aggressive nature of choriocarcinomas in vivo. These cells are also used to investigate the interaction between trophoblastic cells and the maternal immune system, providing insights into immune evasion mechanisms. Additionally, JAR cells have been employed in studies of drug resistance and chemosensitivity, aiding in the development of therapeutic strategies against trophoblastic cancers. As a cell line derived from human tumors, JAR cells are strictly for in vitro research and are not suitable for any in vivo or therapeutic applications.

SKU:BHC11100379

  • Isoenzymes: G6PD, B, PGM1, 1-2, PGM3, 1-2, ES-D, 2, AK-1, 1, GLO-1, 1, Phenotype Frequency Product: 0.0002
  • Products: Estrogen, progesterone, hCG, human chorionic somatomammotropin (placental lactogen), hCG production averages 22.5 ng/ml after reculturing
  • 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
  • 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: Every 3 days
  • 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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