Mouse Anti-KRT3 Recombinant Antibody (AE5) (CBMAB-K1871-LY)

Takan, I., Karakülah, G., Louka, A., & Pavlopoulou, A. (2023). “In the light of evolution:” keratins as exceptional tumor biomarkers. PeerJ, 11, e15099.

Ho, M., Thompson, B., Fisk, J. N., Nebert, D. W., Bruford, E. A., Vasiliou, V., & Bunick, C. G. (2022). Update of the keratin gene family: evolution, tissue-specific expression patterns, and relevance to clinical disorders. Human Genomics, 16(1), 1-21.

Li, C., Shi, Y., Zuo, L., Xin, M., Guo, X., Sun, J., ... & Zhao, H. (2022). Identification of biomarkers associated with cancerous change in oral leukoplakia based on integrated transcriptome analysis. Journal of Oncology, 2022.

Abad-Morales, V., Barbany, M., Gris, O., Güell, J. L., & Pomares, E. (2021). Coexistence of meesmann corneal dystrophy and a pseudo-unilateral lattice corneal dystrophy in a patient with a novel pathogenic variant in the keratin K3 gene: a case report. Cornea, 40(3), 370.

Latta, L., Knebel, I., Bleil, C., Stachon, T., Katiyar, P., Zussy, C., ... & Szentmáry, N. (2021). Similarities in DSG1 and KRT3 Downregulation through Retinoic Acid Treatment and PAX6 Knockdown Related Expression Profiles: Does PAX6 Affect RA Signaling in Limbal Epithelial Cells?. Biomolecules, 11(11), 1651.

Dong, P. N., Cung, L. X., Sam, T. K., Hang, D. T. T., Chung, D. D., Alkadi, T. A., ... & Aldave, A. J. (2020). Identification of a novel missense KRT12 mutation in a Vietnamese family with Meesmann corneal dystrophy. Case Reports in Ophthalmology, 11(1), 120-126.

da Mata Martins, T. M., da Silva Cunha, P., Rodrigues, M. A., de Carvalho, J. L., de Souza, J. E., de Carvalho Oliveira, J. A., ... & de Goes, A. M. (2020). Epithelial basement membrane of human decellularized cornea as a suitable substrate for differentiation of embryonic stem cells into corneal epithelial-like cells. Materials Science and Engineering: C, 116, 111215.

Nishino, T., Kobayashi, A., Mori, N., Masaki, T., Yokogawa, H., Fujiki, K., ... & Sugiyama, K. (2019). In vivo histology and p. L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy. Japanese Journal of Ophthalmology, 63, 46-55.

Ehrlich, F., Laggner, M., Langbein, L., Burger, P., Pollreisz, A., Tschachler, E., & Eckhart, L. (2019). Comparative genomics suggests loss of keratin K24 in three evolutionary lineages of mammals. Scientific reports, 9(1), 10924.

Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols