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MDA-MB-468 Cell Line

General Information
OrganismHomo sapiens, human
Cell Line DescriptionMDA-MB-468 is a cell line that was isolated in 1977 from a 51-year-old woman and is commonly used in breast cancer research. The cells are characterized by their epithelial morphology and are known for their high degree of aneuploidy. MDA-MB-468 cells are estrogen receptor negative (ER-) and are commonly used as a model for studying triple-negative breast cancer (TNBC), a subtype of breast cancer that lacks expression of estrogen receptors (ER), progesterone receptors (PR), and HER2/neu. This makes MDA-MB-468 an important tool for studying cancers that do not respond to hormone therapy or HER2-targeted therapies. Genetically, MDA-MB-468 cells exhibit mutations in the TP53 gene, which is common in various forms of cancer and plays an important role in cell cycle regulation and apoptosis. The cell line also exhibits amplification of the epidermal growth factor receptor (EGFR) gene, which facilitates the study of the EGFR signaling pathway and its impact on cancer progression and treatment resistance.
TissueBreast; Mammary gland
DiseaseAdenocarcinoma
MorphologyEpithelial
GenderFemale
Age51 years
Product FormatFrozen
Growth ModeAdherent
Biosafety Level1
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.
Applications1. Cancer research
2. Drug discovery and testing
3. Molecular and cellular biology research
4. Biomarker identification
5. Genetic studies
6. Mechanistic studies
7. Immunotherapy research
Shipped InDry ice
Storage Temperature−196°C
Additional InfoIn addition to genetic and phenotypic characteristics, MDA-MB-468 cells are also known for their ability to form xenografts in immunocompromised mice, making them a valuable model for studying tumor growth and metastasis in vivo. The responsiveness of this cell line to various chemotherapeutic agents and targeted therapies has been extensively studied to develop effective TNBC treatment strategies.
Characteristics
KaryotypeModal number = 64; range = 60 to 67.
The cell line is an aneuploid human, presumed female (X, abnormal X), with most chromosome numbers in the subtriploid range.
Antigen ExpressionBlood Type AB; HLA Aw23, Aw30, B27, Bw35, Cw2, Cw4 (patient)
Expression MarkersEpidermal growth factor (EGF); transforming growth factor alpha (TGF alpha)
TumorigenicYes, in nude mice.
Mycoplasma TestNegative
Culture Conditions and Handling
Subculturing1. Remove old medium from adhered cells and wash with PBS without calcium and magnesium. For T25 flasks, use 3-5 ml PBS and for T75 flasks, use 5-10 ml.
2. Then completely cover the cells with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks.
3. Let the cells incubate at room temperature for 8-10 minutes to allow them to detach.
4. After incubation, gently mix the cells with 10 ml medium to resuspend, then centrifuge at 300xg for 3 minutes.
5. Discard the supernatant, resuspend the cells with fresh medium, and transfer them to a new flask already containing fresh medium.
Medium Renewal2 to 3 times per week
Subcultivation RatioThe ratio of 1:2 to 1:4 is recommended.
Culture MediumL-15 Medium + 10% FBS
Culture ConditionsAtmosphere: Air, 100%; Temperature: 37°C
CryopreservationComplete growth medium supplemented with 5% (v/v) DMSO

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