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Species | Human |
Cat.No | ABC-HP013X |
Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
Product Category | Primary Cells |
Size/Quantity | 1 vial |
Cell Type | Breast Cell |
Shipping Info | Dry Ice |
Growth Conditions | 37 ℃, 5% CO2 |
Source Organ | Breast |
Disease | Breast Cancer |
Storage | Liquid Nitrogen |
Product Type | Mammary Cells |
Key Features | -Backed by AcceGen advanced technology |
Human Breast Tumor Cancer Cells are derived from malignant breast tissue obtained through surgical resection or biopsy of human patients. They are typically obtained from female patients aged 30-70 years. These cells originate from the epithelial layer of mammary ducts or lobules, with the most common histological subtypes being invasive ductal carcinoma (IDC) and invasive lobular carcinoma (ILC) . Upon isolation, they exhibit characteristic tumorigenic morphology including irregular cell shape, loss of polarity, and formation of disorganized clusters rather than structured acini. Genetically, these cells often harbor mutations in tumor suppressor genes such as TP53 and BRCA1/2, and show amplification of oncogenes like HER2 (ERBB2). They express epithelial markers including cytokeratins (CK7, CK8/18) and breast cancer-associated markers such as estrogen receptor (ER), progesterone receptor (PR), and HER2. Their growth pattern is anchorage-independent. These cells demonstrate aggressive proliferative capacity combined with apoptosis resistance, which significantly contributes to their metastatic potential in vivo..
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
Human Breast Tumor Cancer Cells can be used to explore tumorigenesis mechanisms, gene mutations, abnormal signaling pathways (such as ER/PR/HER2 expression), and microenvironment interactions. It can also be used to evaluate the invasiveness, metabolic reprogramming, and immune escape capabilities of cancer cells