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Py230 Cell Line

General Information
Organism Mus musculus, mouse
Cell Line Description Py230 is a murine mammary intraluminal tumor cell line with epithelial-like characteristics. It is derived from spontaneously generated mammary adenocarcinoma in female MMTV-PyMT (mutine mammary tumor virus promoter-driven polyomavirus T antigen) transgenic C57BL/6 mice. This cell line exhibits characteristics similar to normal murine mammary stem cells and is renowned for its lineage plasticity, meaning it can differentiate into intraluminal cells, myoepithelial cells, and alveolar cells upon stimulation. Py230 is an important model for studying the biology, tumor progression, and immune microenvironment of triple-negative breast cancer (TNBC).
Tissue Mammary gland (Breast)
Disease Mammary Gland Malignant Neoplasm (Mammary adenocarcinoma)
Morphology Epithelial-like; cuboidal-shaped cells that grow in well-differentiated colonies at confluence
Gender Female
Age Adult
Product Format Frozen
Growth Mode Adherent
Biosafety Level 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Applications 1. Triple-negative breast cancer (TNBC) research
2. Study of mammary tumorigenesis and metastatic behavior
3. Investigation of cell state transitions and lineage plasticity
4. Preclinical testing for breast cancer therapeutic strategies
5. Analysis of tumor-immune microenvironment and immunosuppression
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Karyotype Aneuploid (specifically in certain sublines with dysregulated p53); Generally noted for its genetic stability in specific research contexts
Tumorigenic Yes; forms luminal-type primary tumors and lung metastases in syngeneic or immunocompromised mice
Expression Markers Positive for luminal-epithelial markers E-cadherin, Cytokeratin 8, and Cytokeratin 14; Negative for Estrogen Receptor (ER) and Progesterone Receptor (PR) in vitro; Low levels of HER2
Protein Expression Polyoma virus middle T oncogene; p53 (can be nuclear positive in mesenchymal-like sublines)
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Remove and discard the culture medium.
2. Rinse the cell layer with PBS or cell dissociation buffer to remove all serum residue.
3. Add 2.0 to 3.0 mL of trypsin-EDTA solution and observe under a microscope until the cell layer disperses (usually 5 to 15 minutes).
Note: To avoid cell clumping, do not tap or shake the culture flask during cell dissociation.
4. Add 6.0 to 8.0 mL of complete culture medium and gently aspirate the cells using a pipette.
5. Aliquot the cell suspension into new culture containers; a seeding density of 1 × 10^4 to 5 × 10^4 viable cells/cm² is recommended.
Medium Renewal Every other day or 2 to 3 times per week
Subcultivation Ratio A split ratio of 1:3 to 1:6 is recommended
Culture Medium F-12K Medium supplemented with 5% Fetal Bovine Serum (FBS); Some protocols recommend adding MITO+ Serum Extender to maintain differentiation properties.
Culture Conditions Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C
Cryopreservation Complete growth medium supplemented with 5% to 10% (v/v) DMSO

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