| Code | CSB-RA567944A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| IHC | 1:50-1:200 |
PVR, also known as CD155 or Nectin-like protein 5, serves as a critical immunoregulatory molecule that has gained substantial attention in cancer immunology and infectious disease research. Originally identified as the cellular receptor for poliovirus entry, PVR has since emerged as a key player in tumor immune evasion through its interactions with TIGIT and CD96 on immune cells, making it a compelling target for checkpoint immunotherapy studies.
This recombinant monoclonal antibody, generated from clone 19C12, offers researchers the reproducibility and consistency that sequence-defined production provides. Unlike traditional hybridoma-derived antibodies, recombinant technology ensures that each lot delivers identical performance characteristics, eliminating the variability that can compromise longitudinal studies or multi-site collaborations. The rabbit host origin combined with monoclonal specificity yields high-affinity binding to human PVR, developed against a synthetic peptide immunogen.
Validation studies confirm reliable performance across multiple experimental platforms. Western blot analysis of A549 whole cell lysate demonstrates clean detection at the predicted 70 kDa molecular weight, with optimal results achieved at dilutions between 1:500 and 1:2000. This lung adenocarcinoma cell line represents a well-characterized model for PVR expression studies. Immunohistochemistry validation in paraffin-embedded human lung cancer tissue, performed at 1:50 to 1:200 dilutions with citrate buffer antigen retrieval, reveals specific staining patterns suitable for tissue-based investigations.
The affinity-purified antibody arrives in a glycerol-containing buffer optimized for long-term storage stability. For researchers investigating viral pathogenesis, tumor microenvironment dynamics, or immune checkpoint biology, this antibody provides a dependable tool for characterizing PVR expression across cellular and tissue contexts.
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