AR42J cell

SKU:BHC11100120
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Overview
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AR42J cell is a cell line. It is commonly used as an in vitro model for 1 research. Growth characteristics: Cells grow slowly, in clusters and appear as hollow spheroid colonies. They can pile up and attach loosely., Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Disease model Neoplasia
Morphology Epithelial-like
Growth Properties Cells grow slowly, in clusters and appear as hollow spheroid colonies. They can pile up and attach loosely.
Tissue Pancreas tumor, exocrine
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Catalog no. Size
500478 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 500478
Species Rat
AR42J cells are a rat pancreatic tumor cell line derived from azaserine-induced tumors in rats. They are widely used as a model for studying pancreatic exocrine cell functions, pancreatitis, and pancreatic cancer research. AR42J cells exhibit acinar-like characteristics, making them particularly valuable for investigating the physiology and pathology of pancreatic acinar cells. One of the defining features of AR42J cells is their ability to differentiate into cell types exhibiting more pronounced pancreatic exocrine functions when treated with various agents, such as dexamethasone or activators of protein kinase C. Upon differentiation, these cells produce and secrete digestive enzymes, including amylase, lipase, and chymotrypsin, mimicking the enzyme secretion profile of normal pancreatic acinar cells. AR42J cells are also used to explore the mechanisms of acute pancreatitis. They respond to stimuli like cerulein, a cholecystokinin analog, which can induce a condition in the cells that resembles acute pancreatitis, characterized by enzyme overproduction, oxidative stress, and inflammatory responses. This makes AR42J cells a useful tool for testing potential therapeutic interventions for pancreatitis. Furthermore, the AR42J cell line is utilized in research focused on pancreatic cancer, particularly for studies on tumorigenesis and the malignant transformation of acinar cells. They are instrumental in examining the effects of oncogenes, tumor suppressor genes, and growth factors on the development and progression of pancreatic cancer. Overall, AR42J cells provide a versatile and dynamic model system for advancing our understanding of pancreatic diseases and for the development of new therapeutic strategies targeting these conditions.

SKU:BHC11100120

  • Receptors expressed: Insulin, glucocorticoid
  • Tumorigenic: Yes, in athymic mice
  • Products: Amylase and other exocrine enzymes
  • cultureMedium: DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
  • supplements: Supplement the medium with 10% FBS
  • subculturing: It is recommended to cover the tissue culture flasks with gelatine prior to cell cultivation. Gelatine is added to the flask, incubated for 30min at 37 degree Celsius and washed once with PBS. Remove medium and rinse the adherent cells using PBS without calcium and magnesium (3-5 ml PBS for T25, 5-10ml for T75 cell culture flasks). Add Accutase (1-2ml per T25, 2.5ml per T75 cell culture flask), the cell sheet must be covered completely. Incubate at ambient temperature for 8-10 minutes. Carefully resuspend the cells with medium (10 ml), centrifuge for 3 min at 300xg, resuspend cells in fresh medium and dispense into new flasks which contain fresh medium.
  • seedingDensity: 1 x 104 cells/cm2
  • 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 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.
  1. Preparation and Evaluation of [ 18 F]AlF-NOTA-NOC for PET Imaging of Neuroendocrine Tumors: Comparison to [ 68 Ga]Ga-DOTA/NOTA-NOCMolecules| DOI: 10.3390/molecules27206818 | PMC: pmc09609173
  2. (SiFA)SeFe: A Hydrophilic Silicon-Based Fluoride Acceptor Enabling Versatile Peptidic Radiohybrid Tracers.Journal of medicinal chemistry| DOI: 10.1021/acs.jmedchem.4c00924 | PMID: 39115131 | PMC: pm39115131
  3. A sstR2-targeted radiohybrid theranostic agent for PET imaging and β - therapy with excellent preclinical performancenpj Imaging| DOI: 10.1038/s44303-026-00155-w | PMID: 41951775 | PMC: pmc13062086
  4. κB-Ras and Ral GTPases regulate acinar to ductal metaplasia during pancreatic adenocarcinoma development and pancreatitisNature Communications| DOI: 10.1038/s41467-020-17226-0 | PMID: 32641778 | PMC: pmc07343838__41467_2020_17226_MOESM3_ESM
  5. Evaluation of cobalt-labeled octreotide analogs for molecular imaging and auger electron-based radionuclide therapy.Journal of nuclear medicine : official publication, Society of Nuclear Medicine| DOI: 10.2967/jnumed.114.137182 | PMID: 24876207 | PMC: pm24876207
  6. Preparation and Evaluation of [ 18 F]AlF-NOTA-NOC for PET Imaging of Neuroendocrine Tumors: Comparison to [ 68 Ga]Ga-DOTA/NOTA-NOC.Molecules (Basel, Switzerland)| DOI: 10.3390/molecules27206818 | PMID: 36296411 | PMC: pm36296411
  7. Cigarette smoke toxin hydroquinone and misfolding pancreatic lipase variant cooperatively promote endoplasmic reticulum stress and cell deathPLoS ONE| DOI: 10.1371/journal.pone.0269936 | PMID: 35704637 | PMC: pmc09200355

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