For research use only
| Cat No. | ABC-KH1545 |
| Product Type | Knockin Stable Cell Line |
| Species | Human |
| Host Cell | MCF10A |
| Source Organ | Breast |
| Disease | Fibrocystic Disease |
| Storage | Liquid Nitrogen |
Human BRCA1 (185delAG/+) MCF10A Cell Line models hereditary breast cancer for investigating BRCA1 mutation effects on DNA repair and tumor suppressor loss.
Human BRCA1 (185delAG/+) MCF10A Cell line is Heterozygous knockin of 2-bp deletion in BRCA1 resulting in a premature termination codon at position 39.
| Species | Human |
| Cat.No | ABC-KH1545 |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Breast |
| Disease | Fibrocystic Disease |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Knockin Stable Cell Line |
| Host Cell | MCF10A |
| Stock | Custom |
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
The designation “Fibrocystic Disease” reflects the origin of the parental MCF10A cell line rather than a limitation of its research applications. MCF10A is a spontaneously immortalized, non-tumorigenic human mammary epithelial cell line derived from benign breast tissue with fibrocystic changes, which is why it was classified as such in its original description. The cell line retains many characteristics of normal mammary epithelial cells and does not form tumors in vivo.
The introduction of the pathogenic BRCA1 185delAG heterozygous mutation into this near-normal cellular background is intended to model the early cellular state of breast epithelial cells in BRCA1 mutation carriers. This system enables investigation of early cancer-related processes, including increased genomic instability and susceptibility to malignant transformation under additional stresses such as secondary genetic alterations or oxidative damage.
In this context, “fibrocystic disease” denotes the tissue origin, while “BRCA1 (185delAG/+)” defines the key oncogenic genetic alteration. Together, these characteristics make this cell line a biologically relevant model for studying the initiation and early development of breast cancer.