Rabbit Anti-LIM2 Monoclonal Antibody (EPR16947) (CBMAB-1380-YC)

Berry, V., Fujinami, K., Mochizuki, K., Iwata, T., Pontikos, N., Quinlan, R. A., & Michaelides, M. (2022). A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. Ophthalmic Genetics, 43(5), 622-626.

Wang, X., Qin, Y., Abudoukeremuahong, A., Dongye, M., Zhang, X., Wang, D., ... & Lin, H. (2021). Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts. Annals of Translational Medicine, 9(3).

Pei, R., Liang, P. F., Ye, W., Li, J., Ma, J. Y., & Zhou, J. (2020). A novel mutation of LIM2 causes autosomal dominant membranous cataract in a Chinese family. International Journal of Ophthalmology, 13(10), 1512.

Berry, V., Pontikos, N., Dudakova, L., Moore, A. T., Quinlan, R., Liskova, P., & Michaelides, M. (2020). A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract. Ophthalmic genetics, 41(2), 131-134.

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)
Proteogenomic
Other Protocols

Isotype control