A Novel Anti-Cadherin-19 Monoclonal Antibody (Ca19Mab-8) for Flow Cytometry, Western Blotting, and Immunohistochemistry
The type II cadherin Cadherin-19 (CDH19) plays a crucial role in neural crest development. CDH19 regulates cell-cell junctions and migration by forming catenin-cytoskeleton complexes. Although anti-CDH19 monoclonal antibodies (mAbs) are used for specific applications such as Western blotting and immunohistochemistry (IHC), suitable anti-CDH19 mAbs for flow cytometry are limited. Therefore, developing mAbs that specifically recognize cell-surface-expressed CDH19 is essential for advancing both basic research and therapeutic strategies. Here, novel anti-human CDH19 mAbs (Ca<sub>19</sub>Mabs) were created using flow cytometry-based high-throughput screening. One clone, Ca<sub>19</sub>Mab-8 (IgG<sub>1</sub>, κ), specifically recognized CDH19-overexpressed Chinese hamster ovary-K1 cells but did not bind to other 21 CDHs (including both type I and type II CDHs) in flow cytometry. Additionally, Ca<sub>19</sub>Mab-8 recognized endogenous CDH19 in the human glioblastoma cell line LN229. The dissociation constant (<i>K</i><sub>D</sub>) of Ca<sub>19</sub>Mab-8 for LN229/CDH19 was 9.0 × 10<sup>-9</sup> M. Ca<sub>19</sub>Mab-8 also detected endogenous CDH19 in Western blotting. Furthermore, Ca<sub>19</sub>Mab-8 can detect CDH19 in IHC using human melanoma tissue. These findings suggest that Ca<sub>19</sub>Mab-8 is a novel mAb that detects cell-surface-expressed CDH19 with high specificity and is suitable for various applications in basic research. Therefore, Ca<sub>19</sub>Mab-8 has potential for clinical diagnosis and tumor therapy.
Authors
- Mika K. Kaneko (ORCID: https://orcid.org/0000-0002-4158-9208)
- Guanjie Li
- Yukinari Kato
- Hiroyuki Suzuki
Institutions
- Tohoku University (JP)
Publication Details
- Journal
- Current Issues in Molecular Biology
- Published
- 2026-03-12
- DOI
- https://doi.org/10.3390/cimb48030307
- Primary Topic
- Wnt/β-catenin signaling in development and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00