TAS2R5 is a G protein-coupled receptor (GPCR) involved in bitter taste perception and extraoral signaling. The antibody targets a peptide epitope within residues 178–227 of the human TAS2R5 protein, ensuring specificity . Its molecular weight is approximately 34.5 kDa, as confirmed by western blot .
The HRP-conjugated TAS2R5 antibody has been utilized in Alzheimer’s disease (AD) research to quantify protein levels in the orbitofrontal cortex (OFC). Key findings include :
Progressive reduction in TAS2R5 protein levels starting at Braak stage II (early AD) through Braak V (advanced AD).
Correlation with mRNA downregulation, suggesting epigenetic silencing precedes protein loss.
Cellular localization: Expressed in neurons, astrocytes, and brain microvascular endothelial cells .
While primarily validated for ELISA, polyclonal TAS2R5 antibodies (non-conjugated) show reactivity in WB at dilutions of 1:500–1:2000 . HRP conjugation enhances sensitivity for low-abundance targets.
Epigenetic regulation: H3K9me3 histone modifications and MeCP2 interactions at TAS2R5 promoters correlate with transcriptional repression in early AD .
Protein levels: Reduced by >50% in advanced AD stages compared to non-demented controls .
Though not directly studied, TAS2R14 (a related bitter receptor) shows prognostic significance in papillary thyroid carcinoma (PTC):
Higher TAS2R14 expression correlates with improved progression-free survival () .
TAS2R agonists induce apoptosis in PTC cells, suggesting therapeutic potential for TAS2R-targeted therapies .
Specificity: Verified via peptide-blocking assays and cross-reactivity tests .
Reproducibility: Batch-to-batch consistency confirmed by stain-free total protein normalization in WB .
Storage: Stable at -20°C long-term; avoid freeze-thaw cycles .
| Vendor | Product Code | Conjugate | Applications |
|---|---|---|---|
| Cusabio | CSB-PA885769PB01HU | HRP | ELISA |
| Boster Bio | A11429 | None | ELISA, WB |
| Atlas Antibodies | HPA053742 | None | IHC, ICC-IF, WB |
Sensitivity: HRP conjugation limits multiplexing compared to fluorophore-labeled alternatives.
Tissue specificity: Limited data outside neuronal and endocrine tissues.
Therapeutic potential: Mechanistic studies linking TAS2R5 signaling to disease pathways remain sparse.