
- Tissue
- Mammary gland
- Disease
- Malignant neoplasms of the mouse mammary gland
- Synonyms
- P years8119
Documents
PY8119-GFP
Cell line · Product number 305857
PY8119-GFP cells are a fluorescently labeled derivative of the murine PY8119 breast cancer cell line, which originates from a spontaneous mammary tumor in...
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01General information
- Description
PY8119-GFP cells are a fluorescently labeled derivative of the murine PY8119 breast cancer cell line, which originates from a spontaneous mammary tumor in a mouse model. The parental PY8119 line is commonly associated with genetically engineered mouse models of breast cancer and is used to study tumor progression, immune interactions, and therapeutic responses in a syngeneic context. Stable expression of green fluorescent protein (GFP) enables direct visualization of tumor cell behavior, facilitating real-time tracking of proliferation, migration, and cellular interactions both in vitro and in vivo.
The GFP modification makes PY8119-GFP cells particularly well suited for applications such as live-cell imaging, intravital microscopy, and metastasis studies in immunocompetent mouse models. These cells retain key characteristics of the parental line, including aggressive growth and the ability to form tumors when implanted into syngeneic hosts. As a result, PY8119-GFP cells are widely used to investigate tumor–immune system dynamics, evaluate anti-cancer therapies, and study mechanisms of invasion and dissemination. However, as with all fluorescently modified lines, careful validation is recommended to ensure that GFP expression does not alter baseline cellular behavior.
Genetic modification: Stably modified by replication-incompetent lentiviral transduction to express the ZsGreen1 green fluorescent protein reporter; maintained as a polyclonal population under puromycin selection (1–5 µg/mL). S1/BSL-1 containment.
- Tissue
- Mammary gland
- Disease
- Malignant neoplasms of the mouse mammary gland
- Synonyms
- P years8119
02Classification
- Organism
- Mouse
- Sex
- Female
- Growth properties
- Adherent
- GMO status
- GMO-S1
- GMO status details
- GMO-S1: This cell line contains a stably integrated ZsGreen1 green fluorescent protein reporter introduced via replication-incompetent lentiviral transduction. The resulting polyclonal cell population was maintained under puromycin selection (1–5 µg/mL). S1 containment is required. This classification applies only within Germany and may differ elsewhere.
- Biosafety level
- 1
03Characteristics
- Morphology
- Epithelial-like
- Cell type
- Mesenchymal-like cell
04Identifiers
- Citation
- PY8119-GFP (Cytion catalog number 305857)
- NCBI TaxID
- 10090
05Expression and susceptibility
- Antigen expression
- ZsGreen1 (green fluorescent protein)
06Handling and culture
- Culture medium
- 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)
- Incubation atmosphere
37°C, 5% CO2, humidified atmosphere.
- Supplements
- Supplement the medium with 10% FBS
- Seeding density
- 1.5-4 X 104 cells/cm2
- Fluid renewal
- 2 to 3 times per week
- Thawing and culturing
Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.
Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.
For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.
Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.
Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.
Centrifuge the mixture at 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.
Follow the procedure described under Post-Thaw Recovery
07Quality control and cryopreservation
- Freeze medium
- As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
- Storage conditions
For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.
- Shipping conditions
Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.
08Donor
- Donor age
- Adult
09Legal and safety
- Safety precautions
- When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments.
- Warranty
At Cytion, we stand behind the quality and viability of our products. We guarantee that our cells will be viable at the start of culture for 60 days after shipment from our facilities. We assure that all materials conform to the specifications described in the Certificate of Analysis and/or Product Sheet.
For full details, please refer to our Warranty Statement.
- Material Transfer Agreement required
- Yes