Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-SC004948
Host Cell : HEK293 (CHO and other cell types are also available) Size : >1x106 frozen cells/vial
| Cat. No. | CSC-SC004948 |
| 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 | ENPP3 |
| 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 | ENPP3 ectonucleotide pyrophosphatase/phosphodiesterase 3 [ Homo sapiens ] |
| Gene Symbol | ENPP3 |
| Synonyms | B10; NPP3; PDNP3; CD203c; PD-IBETA |
| Gene Description | ectonucleotide pyrophosphatase/phosphodiesterase 3 |
| GeneID | 5169 |
| Uni ProtID | O14638 |
| mRNA Refseq | NM_005021.3 |
| Protein Refseq | NP_005012.2 |
| Chromosome Location | 6q22 |
| Function | NADH pyrophosphatase activity; metal ion binding; nucleic acid binding; nucleoside-triphosphate diphosphatase activity; nucleotide diphosphatase activity; phosphodiesterase I activity; polysaccharide binding; scavenger receptor activity; |
| Pathway | Nicotinate and nicotinamide metabolism, organism-specific biosystem; Nicotinate and nicotinamide metabolism, conserved biosystem; Pantothenate and CoA biosynthesis, organism-specific biosystem; Pantothenate and CoA biosynthesis, conserved biosystem; Purine metabolism, organism-specific biosystem; Purine metabolism, conserved biosystem; Riboflavin metabolism, organism-specific biosystem; |
| MIM | 602182 |
Mounting evidence suggests that aberrant methylation plays a crucial role in the development and progression of endometriosis (EMs). Here, researchers investigated the relationship between aberrant ENPP3 promoter methylation and the pathogenesis of ovarian EMs, focusing on its regulatory role on ENPP3 expression. Results showed that the methylation level of the CpG site in the ENPP3 promoter region was significantly reduced in ectopic endometrial tissue compared to normal endometrial tissue. RT-qPCR results revealed significantly increased ENPP3 expression in ovarian EMs tissue compared to endometrial tissue from patients without EMs, and this upregulation was negatively correlated with the methylation level of the ENPP3 promoter region. Immunohistochemical analysis confirmed increased ENPP3 expression in glandular epithelial cells and stroma of ovarian EMs tissue. Furthermore, in vitro experiments showed that overexpression of ENPP3 significantly enhanced the invasion and migration capabilities of endometrial stromal cells. Transcriptome sequencing and functional analysis indicated that increased ENPP3 expression activated the AKT/mTOR/4EBP1 signaling pathway. In summary, this study suggests that hypomethylation of the ENPP3 promoter region may promote the occurrence and development of ovarian endometriosis by activating the AKT/mTOR/4EBP1 pathway, supporting the theory that endometriosis may be an epigenetically regulated disease.
Transwell chamber migration assay was used to evaluate the migration and invasion abilities of cells. The results showed that the migration and invasion abilities of ENPP3-overexpressing human endometrial stromal cells (HESCs) were significantly enhanced (Figure 1).
Figure 1. Overexpression of ENPP3 promoted cell migratory and invasive capabilities. (Qin Y, et al., 2024)
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