mProX™ Human SIGLEC14 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Immune Checkpoint Cell Lines
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Published Data
Fig.1 The potential for cross-reactivity between Siglec-5 monoclonal antibodies and Siglec-14 is being investigated.
Cells transfected with Siglec-14/pIRES2-EGFP (dotted line), Siglec-5/pIRES2-EGFP (solid line), or pIRES2-EGFP (shaded) were probed with available monoclonal antibodies and subjected to analysis via flow cytometry. The populations that were positive for green fluorescent protein were gated and subsequently plotted. Both Siglec-5 and Siglec-14 were recognized by most monoclonal antibodies, with the exception of clone 194117.
Ref: Angata, Takashi, et al. "Discovery of Siglec-14, a novel sialic acid receptor undergoing concerted evolution with Siglec-5 in primates." The FASEB Journal 20.12 (2006): 1964-1973.
Pubmed: 17012248
DOI: 10.1096/fj.06-5800com
Research Highlights
G Ovsyannikova, Inna. et al. "Genome-wide determinants of cellular immune responses to mumps vaccine." Vaccine, 2023.
The authors of this study have previously examined the role of genetic variations in certain candidate genes in influencing differences in antibody responses to mumps vaccination among individuals. Building on this previous research, they conducted a genome-wide association study (GWAS) to identify potential genetic variants that may impact cellular immune responses to mumps vaccines. These findings have the potential to further our understanding of the complex factors that contribute to variations in vaccine efficacy.
G Ovsyannikova, Inna. et al. "Genome-wide determinants of cellular immune responses to mumps vaccine." Vaccine, 2023.
Pubmed:
37778899
DOI:
10.1016/j.vaccine.2023.09.001
K, Michelle; J, Christopher. "Carbon nanotubes activate inflammatory signalling through binding to Siglec-14." Nature nanotechnology, 2023.
This article is a commentary on a recent study by Yamaguchi et al. that showed how carbon nanotubes can trigger inflammation by binding to a receptor called Siglec-14 on immune cells. The authors discuss the implications of this finding for nanotoxicology and nanomedicine, as well as the potential role of Siglec-14 in other diseases such as COVID-19 and tuberculosis. They also suggest some strategies to reduce the inflammatory effects of carbon nanotubes by modifying their surface properties or blocking Siglec-14.
K, Michelle; J, Christopher. "Carbon nanotubes activate inflammatory signalling through binding to Siglec-14." Nature nanotechnology, 2023.
Pubmed:
37316701
DOI:
10.1038/s41565-023-01420-4