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-SC000591
Host Cell : HEK293 (CHO and other cell types are also available) Size : >1x106 frozen cells/vial
| Cat. No. | CSC-SC000591 |
| 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 | ANGPT1 |
| 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 | ANGPT1 angiopoietin 1 [ Homo sapiens ] |
| Gene Symbol | ANGPT1 |
| Synonyms | AGP1; AGPT; ANG1 |
| Gene Description | angiopoietin 1 |
| GeneID | 284 |
| Uni ProtID | Q15389 |
| mRNA Refseq | NM_001146.3 |
| Protein Refseq | NP_001137.2 |
| Chromosome Location | 8q23.1 |
| Function | receptor tyrosine kinase binding; |
| Pathway | Angiogenesis, organism-specific biosystem; Angiopoietin receptor Tie2-mediated signaling, organism-specific biosystem; Cell surface interactions at the vascular wall, organism-specific biosystem; HIF-1 signaling pathway, organism-specific biosystem; Hemostasis, organism-specific biosystem; PI3K-Akt signaling pathway, organism-specific biosystem; PI3K-Akt signaling pathway, conserved biosystem; |
| MIM | 601667 |
Angiopoietin-1 (ANG1, also known as ANGPT1) is a pro-angiogenic regulatory factor that drives the progression of solid tumors by stimulating the proliferation, migration, and lumen formation of vascular endothelial cells, as well as by promoting vascular remodeling and stabilization. However, the function and underlying mechanisms of ANG1 in triple-negative breast cancer (TNBC) remain unclear. Clinical data indicate that elevated ANG1 levels in TNBC are associated with a poor prognosis compared to non-TNBC. Furthermore, ANG1 knockdown inhibits TNBC cell proliferation and induces G1 phase cell cycle arrest and apoptosis, whereas ANG1 overexpression promotes tumor growth in nude mice. Mechanistic studies reveal that ANG1 facilitates TNBC progression by upregulating the expression of carboxypeptidase A4 (CPA4). In summary, the ANG1-CPA4 axis represents a potential therapeutic target for TNBC.
To investigate the effect of ANG1 on triple-negative breast cancer (TNBC), researchers examined ANG1 expression in TNBC cell lines and selected four lines for subsequent study. They knocked down ANG1 in Hs578T and SUM149PT cells, which exhibit high ANG1 protein levels (Figure 1A), and overexpressed ANG1 in HCC1806 and MDA-MB-468 cells, which exhibit low ANG1 protein levels (Figure 1E). SRB and colony formation assays demonstrated that proliferation was inhibited in ANG1-knockdown Hs578T and SUM149PT cells (Figure 1B-D), whereas it was significantly promoted in ANG1-overexpressing HCC1806 and MDA-MB-468 cells (Figure 1F, G).
Figure 1. ANG1 promotes the proliferation of TNBC cells. (Liu X, et al., 2023)
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