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Human EPOR-JAK2 Stable Cell Line - Ba/F3

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RO1114M

Host Cell :   Ba/F3 Size :   >1x106 frozen cells/vial

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Cell Line Information

Cell Culture Information

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Gene Information

Cat. No. CSC-RO1114M
Description Ba/F3-EPOR-JAK2 cell line is engineered to stably overexpress exogenous human EPOR-JAK2.
Target Gene EPOR-JAK2
Gene Species Homo sapiens (Human)
Host Cell Ba/F3
Host Cell Species Mus musculus (Mouse)
Applications Drug screening and biological assays
Biosafety Level 2
Size >1x10^6 frozen cells/vial, 1 mL
Stability Stable in culture over a minimum of 10 passages
Quality Control Negative for bacteria, yeast, fungi and mycoplasma.
Growth Conditions 37 °C, 5% CO2
Storage Liquid nitrogen
Shipping Dry ice
Thawing & Subculturing Instructions 1. Thaw cells by gently swirling in a 37°C water bath. To limit contamination, do not submerge the O-ring and cap. 2. When cells are ~70% thawed (~1 min), transfer the vial into a biosafety cabinet, and wipe the surface with 70% ethanol. Allow tube to dry completely. 3. Transfer the cells gently into a 15 mL conical tube containing 10 mL of pre-warmed culture medium (without antibiotic selection marker). Centrifuge cells at ~125 x g for 5~7 min. 4. Remove supernatant without disturbing the pellet, and resuspend cells in 1 mL culture medium (without antibiotic selection marker). Transfer cells to a 6-well plate containing ~2 mL pre-warmed growth medium (without antibiotic selection marker) or a T25 flask containing 5 mL pre-warmed culture medium (without antibiotic selection marker). 5. Incubate the culture at 37°C with 5% CO2. 6. Subculture: split saturated culture 1:4 ~ 1:6 every 3 days; seed out at about 1~3 x 10^5 cells/mL.
Freeze Medium Frozen with 70% medium, 20% FBS, 10% DMSO
Growth Properties Suspension, round
Freezing Instructions Cells are recommended to generate additional frozen stocks at early passages. Frozen stocks should be preserved in a designated cryopreservation medium or in 70% RPMI 1640 + 20% FBS + 10% DMSO (without antibiotic selection marker). 1. Prepare the freezing medium (70% RPMI 1640 + 20% FBS + 10% DMSO, without antibiotic selection marker) fresh immediately before use. 2. Keep the freezing medium on ice and label cryovials. 3. Transfer cells to a sterile, conical centrifuge tube, and count the cells. 4. Centrifuge the cells at 250 x g for 5 minutes at room temperature and carefully aspirate off the medium. 5. Resuspend the cells at a density of at least 3 x10^6 cells/ml in chilled freezing medium. 6. Aliquot 1 ml of the cell suspension into each cryovial. 7. Freeze cells in the CoolCell freezing container overnight in a -80°C freezer. 8. Transfer vials to liquid nitrogen for long-term storage.
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations The following safety precautions should be observed.
1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
2. No eating, drinking or smoking while handling the stable line.
3. Wash hands after handling the stable line and before leaving the lab.
4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.
5. All waste should be considered hazardous.
6. Dispose of all liquid waste after each experiment and treat with bleach.
Ship Dry ice
Target Gene EPOR-JAK2
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The erythropoietin receptor (EPOR) is a transmembrane protein belonging to the cytokine receptor superfamily. Upon binding to erythropoietin (EPO), EPOR undergoes a conformational change that activates the associated Janus kinase 2 (JAK2), a cytoplasmic tyrosine kinase that initiates downstream signaling cascades including the JAK2-STAT5, PI3K-AKT, and MAPK pathways. This signaling axis is essential for erythroid progenitor cell survival, proliferation, and differentiation, and its dysregulation is implicated in various hematological disorders such as polycythemia vera, primary myelofibrosis, and certain erythroleukemias. The Human EPOR-JAK2 Stable Cell Line - Ba/F3 is generated by stably transfecting the murine IL-3-dependent pro-B cell line Ba/F3 with expression constructs encoding human EPOR and JAK2. Ba/F3 cells are naturally IL-3 dependent and do not express endogenous EPOR, making them an ideal null background for studying exogenous cytokine receptor signaling. Expression of human EPOR and JAK2 in these cells enables EPO-dependent proliferation, effectively replacing the IL-3 requirement and providing a clean, controllable system for functional studies.

This cell line is widely used in preclinical drug discovery and basic research applications. It serves as a valuable tool for screening and characterizing small molecule inhibitors targeting JAK2, particularly those designed for the treatment of myeloproliferative neoplasms and other JAK2-driven malignancies. Researchers can evaluate compound potency, selectivity, and cytotoxicity by monitoring EPO-dependent cell proliferation using standard viability assays such as MTT, CellTiter-Glo, or Alamar Blue. The cell line is also suitable for mechanistic studies of JAK2 signal transduction, including phosphorylation profiling of downstream effectors like STAT5, STAT3, and ERK1/2 via western blotting or ELISA-based readouts. Additionally, it can be used to assess the functional impact of EPOR or JAK2 mutations identified in patient samples, or to study resistance mechanisms that arise under therapeutic pressure. Beyond oncology, the cell line supports research into EPO biology, erythropoiesis regulation, and the development of biosimilar EPO therapeutics.

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Customer Reviews
Perfect for Cytokine-Independent Assays

This EPOR-JAK2 Ba/F3 line transitioned flawlessly to IL-3 independent growth upon arrival. We use it regularly for testing novel JAK inhibitors, and the signal-to-background ratio in our luminescent viability assays is outstanding. Great quality control and documentation.

Australia

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