Rat Anti-MFRP (AA 101-579) Recombinant Antibody (CBFYM-2160) (CBMAB-M2342-FY)

Mora-Roldan, G. A., Nava, J., Gazarian, K., & Zenteno, J. C. (2024). Generation of the induced pluripotent stem cell line IOCVi001-A from a patient with the MFRP-related retinitis pigmentosa-nanophthalmos syndrome. Stem Cell Research, 103309.

Aucoin, A., Guerin, M. A. K., Gordon, W. C., Ji, J., Perera, R., Elison, J., ... & Bazan, N. G. (2023). Deletion of membrane-type frizzled-related protein (MFRP) or adiponectin receptor 1 (AdipoR1) results in selective fatty acid synthesis impairments and photoreceptor cell degeneration in mice. Investigative Ophthalmology & Visual Science, 64(8), 4866-4866.

Tian, X., Zheng, Q., Xie, J., Zhou, Q., Liang, L., Xu, G., ... & Lu, D. (2023). Improved gene therapy for MFRP deficiency-mediated retinal degeneration by knocking down endogenous bicistronic Mfrp and Ctrp5 transcript. Molecular Therapy-Nucleic Acids, 32, 843-856.

Woodard, D., Dang, K., Lancione, R., Biswas, P., Lazaro, D., Dinov, A., ... & Ayyagari, R. (2023). Single-nucleus multi-modal analysis of photoreceptor alterations during cellular stress in MFRP-associated retinal degeneration. Investigative Ophthalmology & Visual Science, 64(8), 1862-1862.

Ren, X., Gao, Y., Lin, Y., Fu, X., Xiao, L., Wang, X., ... & Tang, L. (2022). A novel mutation in the membrane frizzled-related protein gene for posterior microphthalmia, non-pigmented retinitis pigmentosa, optic nerve drusen, and retinoschisis in a consanguineous family. Frontiers in Medicine, 9, 835621.

Chiou, C. A., Rajabi, F., Fulton, A. B., Acsadi, G., Waitzman, D. M., & Gaier, E. D. (2022). Membrane Frizzled-Related Protein-Related Disease Mimicking Idiopathic Intracranial Hypertension. Journal of Neuro-Ophthalmology, 10-1097.

Pachauri, S., Dang, K., Biswas, P., Chekuri, A. K., Dagar, M., Berry, A. M., ... & Ayyagari, R. (2022). Single-nucleus multi-modal analysis of MFRP associated retinal degeneration. Investigative Ophthalmology & Visual Science, 63(7), 7-7.

Kautzmann, M. A. I., Gordon, W. C., Jun, B., Do, K. V., Matherne, B. J., Fang, Z., & Bazan, N. G. (2020). Membrane‐type frizzled‐related protein regulates lipidome and transcription for photoreceptor function. The FASEB Journal, 34(1), 912.

Godinho, G., Madeira, C., Grangeia, A., Neves-Cardoso, P., Santos-Silva, R., Brandão, E., ... & Estrela-Silva, S. (2020). A novel MFRP gene variant in a family with posterior microphthalmos, retinitis pigmentosa, foveoschisis, and foveal hypoplasia. Ophthalmic Genetics, 41(5), 474-479.

Morillo Sanchez, M. J., Llavero Valero, P., González-Del Pozo, M., Ponte Zuniga, B., Antiñolo, G., Ramos Jimenez, M., & Rodríguez De La Rúa Franch, E. (2019). Posterior microphthalmos, retinitis pigmentosa, and foveoschisis caused by a mutation in the MFRP gene: a familial study. Ophthalmic Genetics, 40(3), 288-292.

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