For research use only
| Cat No. | ABC-X0144C |
| Product Type | Overexpression Stable Cell Lines |
| Cell Type | Epithelial-like |
| Species | Human |
| Host Cell | MC38 |
| Source Organ | Colon |
| Disease | Colon Adenocarcinoma |
| Storage | Liquid Nitrogen |
The MMP7 MC38 overexpression cell line is your go-to model for analyzing tumor biology and testing MMP7-targeted therapies in murine systems.
Xpress™ Human MMP7 over-expressing cell line (MC38) is a genetically engineered model derived from selected murine colon adenocarcinoma MC38 parental cell line based on customers’ requirement. MMP7 MC38 overexpression cell line is generated by stable integration of exogenous human MMP7 into MC38 host cells using our optimized transduction of lentiviral vectors. Overexpression clone is validated at gene level by qRT-PCR.
Target
The MMP7 gene encodes matrix metallopeptidase 7, a zinc-dependent protease that degrades components of the extracellular matrix and is crucial for tissue remodeling, inflammation, and cancer metastasis. MMP7 is overexpressed in colorectal, pancreatic, and lung cancers, where it facilitates invasion, angiogenesis, and tumor growth via ECM breakdown and signaling molecule activation. AcceGen offers generation of stable overexpression cell lines targeting any gene of your interest. Polyclonal or monoclonal is optional based on customers’ research needs.
| Species | Human |
| Cat.No | ABC-X0144C |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial-like |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 °C, 5% CO₂ |
| Source Organ | Colon |
| Disease | Colon Adenocarcinoma |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Overexpression Stable Cell Lines |
| Host Cell | MC38 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The MMP7 MC38 Overexpression Cell Line offers a syngeneic-compatible platform for studying matrix remodeling and immune-tumor interactions in murine models. It is valuable for mechanistic analysis and in vivo drug efficacy testing of MMP7-targeted therapies.