Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-SC009609
Host Cell : HEK293 (CHO and other cell types are also available) Size : >1x106 frozen cells/vial
| Cat. No. | CSC-SC009609 |
| Description | Using Creative Biogene's proprietary lentiviral vectors, we subclone the target gene into lentivector, generate the lentivirus particles, sequentially infect the cell line HEK293 (other cell types are also available according to your requirements), and select the clones constantly expressing target gene at high level. |
| Target Gene | MMP7 |
| Gene Species | Homo sapiens (Human) |
| Host Cell | HEK293 (CHO and other cell types are also available) |
| Host Cell Species | Species varies |
| Applications |
1. Gene expression studies 2. Signaling pathway research 3. Drug screening and toxicology 4. Disease research |
| Size | 2 × 10^6 cells / vial |
| Stability | Validated for at least 10 passages |
| Quality Control | Negative for bacteria, yeast, fungi and mycoplasma. |
| Storage | Liquid nitrogen |
| Shipping | Dry Ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
| Gene Name | MMP7 matrix metallopeptidase 7 (matrilysin, uterine) [ Homo sapiens ] |
| Gene Symbol | MMP7 |
| Synonyms | MMP-7; MPSL1; PUMP-1 |
| Gene Description | matrix metallopeptidase 7 (matrilysin, uterine) |
| GeneID | 4316 |
| Uni ProtID | P09237 |
| mRNA Refseq | NM_002423.3 |
| Protein Refseq | NP_002414.1 |
| Chromosome Location | 11q21-q22 |
| Function | metalloendopeptidase activity; zinc ion binding; |
| Pathway | Activation of Matrix Metalloproteinases, organism-specific biosystem; Alpha6-Beta4 Integrin Signaling Pathway, organism-specific biosystem; Degradation of the extracellular matrix, organism-specific biosystem; Extracellular matrix organization, organism-specific biosystem; Matrix Metalloproteinases, organism-specific biosystem; Syndecan-1-mediated signaling events, organism-specific biosystem; Wnt Signaling Pathway and Pluripotency, organism-specific biosystem; |
| MIM | 178990 |
Matrix metalloproteinase 7 (MMP7), the smallest member of the matrix metalloproteinase family, has been shown to be closely associated with cancer progression, especially metastasis. However, its expression pattern and function in tongue cancer remain unclear. Here, researchers found that MMP7 expression was significantly increased in human tongue squamous cell carcinoma (TSCC) specimens compared to paired non-tumor tissues, and this high expression was closely associated with lymph node metastasis in patients. Furthermore, molecular functional assays confirmed that MMP7 promotes the proliferation, migration, and invasion of TSCC cells. Knockdown of MMP7 inhibited lymph node metastasis in vivo. Therefore, MMP7 plays an oncogenic role in the occurrence and metastasis of tongue cancer and may be a potential therapeutic target for tongue cancer.
Here, researchers constructed MMP7-overexpressing CAL27 and SCC9 cells and validated the results using real-time quantitative PCR (Figure 1a) and Western blotting (Figure 1b). The results of the CCK8 assay (Figure 1c) and clonogenic assay (Figure 1d) showed that MMP7 overexpression accelerated the proliferation process of CAL27 and SCC9 cells.
Figure 1. Overexpression of MMP7 promotes tongue cancer cell line growth in vitro. (Yuan S, et al., 2020)
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