Rabbit Anti-ERLIN2 Recombinant Antibody (1533) (V2LY-0825-LY721)

Wolf, L. M., Lambert, A. M., Haenlin, J., & Boutros, M. (2021). EVI/WLS function is regulated by ubiquitylation and is linked to ER-associated degradation by ERLIN2. Journal of cell science, 134(16), jcs257790.

Park, J. M., Lee, B., Kim, J. H., Park, S. Y., Yu, J., Kim, U. K., & Park, J. S. (2020). An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18). Scientific Reports, 10(1), 1-6.

Liu, Y., Xie, P., Jiang, D., Liu, J., Zhang, J., Bian, T., & Shi, J. (2020). Molecular and immune characteristics for lung adenocarcinoma patients with ERLIN2 overexpression. Frontiers in Immunology, 11, 568440.

Du, F., & Hou, Q. (2020). SNHG17 drives malignant behaviors in astrocytoma by targeting miR-876-5p/ERLIN2 axis. BMC cancer, 20(1), 1-10.

Srivastava, S., D’Amore, A., Cohen, J. S., Swanson, L. C., Ricca, I., Pini, A., ... & Santorelli, F. M. (2020). Expansion of the genetic landscape of ERLIN2‐related disorders. Annals of clinical and translational neurology, 7(4), 573-578.

Muratet, F., Teyssou, E., Banneau, G., Danel-Brunaud, V., Allart, E., Antoine, J. C., ... & Millecamps, S. (2019). Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS. Neurology Genetics, 5(6).

Wright, F. A., Bonzerato, C. G., Sliter, D. A., & Wojcikiewicz, R. J. (2018). The erlin2 T65I mutation inhibits erlin1/2 complex–mediated inositol 1, 4, 5-trisphosphate receptor ubiquitination and phosphatidylinositol 3-phosphate binding. Journal of Biological Chemistry, 293(40), 15706-15714.

Wu, H., Li, J., Luo, S., & Wang, G. (2018). MiR-410 acts as a tumor suppressor in estrogen receptor-positive breast cancer cells by directly targeting ERLIN2 via the ERS pathway. Cellular Physiology and Biochemistry, 48(2), 461-474.

Rydning, S. L., Dudesek, A., Rimmele, F., Funke, C., Krüger, S., Biskup, S., ... & Kamm, C. (2018). A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European Journal of Neurology, 25(7), 943-e71.

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