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Panoply™ Human ACVR2A Knockdown Stable Cell Line

Panoply™ Human ACVR2A Knockdown Stable Cell Line

Cat.No. :  CSC-DC000217

Host Cell:  HEK293 (Hela and other cell types are also available) Validation:  Real-Time RCR

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Cat. No. CSC-DC000217
Description Creative Biogene's Knockdown Cell Lines are target specific shRNA lentivirus transduced cells. The percent knockdown levels range from 75-99% depending on the gene, as evaluated by Real-Time RCR. Cells are rigorously qualified and mycoplasma free.
Gene ACVR2A
Host Cell HEK293 (Hela and other cell types are also available)
Host Cell Species Homo sapiens (Human)
Stability Validated for at least 10 passages
Application

(1) Studying gene functions

(2) Studying gene interactions and signaling pathways

(3) Target validation and drug discovery

(4) Designing diseases models

Quality Control Negative for bacteria, yeast, fungi and mycoplasma.
Size Form >1 × 10^6 cells / vial
Shipping Dry Ice
Storage Liquid Nitrogen
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
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Activin A receptor type 2A (ACVR2A) is a membrane receptor in the transforming growth factor-β (TGF-β) signaling pathway, involved in regulating cell proliferation, migration, and apoptosis. Here, researchers examined the expression profile and biological function of ACVR2A in colon cancer. In the GSE39582 database, ACVR2A mRNA expression was identified as a prognostic factor by linear regression analysis. In a validation cohort of 15 patients with stage IV cancer, ACVR2A mRNA expression was significantly decreased in metastatic lesions and primary tumors compared with adjacent normal controls. In another tissue microarray (TMA) validation cohort of 193 cases, decreased ACVR2A protein expression was associated with advanced N stage and positive lymphovascular invasion. A strong correlation between low ACVR2A mRNA or protein expression and poor survival was also observed in both the GSE39582 database and the TMA validation cohort. Furthermore, in vitro studies demonstrated significantly increased cell migration in ACVR2A knockdown cells. These findings suggest that loss of ACVR2A plays an important role in cancer progression and distant metastasis and may serve as a prognostic marker for patients with colon cancer.

To evaluate the biological function of ACVR2A in colon cancer, the researchers generated stable ACVR2A knockdown RKO and HCT116 cell lines (Figures 1a and b). The results showed that ACVR2A knockdown did not affect colon cancer cell proliferation (Figure 1c). Next, they used Transwell assays to investigate whether ACVR2A knockdown affected colon cancer cell migration. The results showed that the number of migrating cells increased two- to three-fold in the ACVR2A knockdown cell lines compared to the control group (Figure 1d).

Figure 1. Silencing of ACVR2A expression promotes the migration of human colon cancer cells.Figure 1. Silencing of ACVR2A expression promotes the migration of human colon cancer cells. (Zhuo C, et al., 2018)

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