mProX™ Human NECTIN2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Immune Checkpoint Cell Lines
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Published Data
Fig.1 Knockdown of Nectin-2 in ESCC cell lines.
Nectin-2 protein expression was observed to diminish significantly in human esophageal squamous cell carcinoma ECA109 and KYSE510 cell lines following in vitro transfection with Nectin-2 siRNA. The siRNA used, designated as si-nectin-2, specifically targeted Nectin-2, while a control siRNA, referred to as si-con, was employed for comparison in the study.
Ref: Li, Ming, et al. "Elevated Nectin-2 expression is involved in esophageal squamous cell carcinoma by promoting cell migration and invasion." Oncology Letters 15.4 (2018): 4731-4736.
Pubmed: 29552112
DOI: 10.3892/ol.2018.7953
Research Highlights
Ukraintseva, Svetlana. et al. "Vaccination Against Pneumonia May Provide Genotype-Specific Protection Against Alzheimer's Disease." Journal of Alzheimer's disease : JAD, 2023.
The study aims to explore the potential benefits of vaccine repurposing for personalized prevention of Alzheimer's disease (AD) based on individual genotype. A retrospective cohort analysis was conducted using data from the Cardiovascular Health Study, to examine the relationship between receiving pneumococcal polysaccharide vaccine and flu shots between ages 65-75, and the onset of AD at age 75 or older. The rs6859 polymorphism in the NECTIN2 gene, known to increase risk for AD, was taken into consideration. Results showed that carriers of the rs6859 A allele who received pneumococcal vaccine and multiple pneumonia and flu vaccinations had lower odds of developing AD. The study concludes that pneumococcal polysaccharide vaccine shows promise for personalized AD prevention based on genotype.
Ukraintseva, Svetlana. et al. "Vaccination Against Pneumonia May Provide Genotype-Specific Protection Against Alzheimer's Disease." Journal of Alzheimer's disease : JAD, 2023.
Pubmed:
37807778
DOI:
10.3233/JAD-230088
Paolini, Rossella; Molfet, Rosa. "Dysregulation of DNAM-1-Mediated NK Cell Anti-Cancer Responses in the Tumor Microenvironment." Cancers, 2023.
NK cells play a crucial role in the body's defense against cancer by using both inhibitory and activating receptors to regulate their ability to destroy cancerous cells while sparing healthy cells. However, the tumor microenvironment often causes dysfunction in NK cells by reducing activating receptors and increasing inhibitory checkpoint receptors. One essential activating receptor, DNAM-1, plays a critical role in recognizing cancer cells by binding to PVR and Nectin2 adhesion molecules. These same molecules can also activate inhibitory signals through immune checkpoint receptors that are overexpressed in the tumor microenvironment. TIGIT, in particular, has gained attention for its ability to enhance anti-tumor responses by targeting these inhibitory signals. This review will summarize the mechanisms by which PVR and Nectin2 recognition by paired inhibitory and activating receptors regulates NK cell-mediated destruction of cancer cells and discuss potential therapeutic approaches to reverse DNAM-1 dysfunction in the tumor microenvironment.
Paolini, Rossella; Molfet, Rosa. "Dysregulation of DNAM-1-Mediated NK Cell Anti-Cancer Responses in the Tumor Microenvironment." Cancers, 2023.
Pubmed:
37760586
DOI:
10.3390/cancers15184616