Rabbit Anti-EIF1AX Recombinant Antibody (CBFYE-0635) (V2LY-0425-LY1628)

French, E. K., Nikitski, A. V., Yip, L., Nikiforova, M. N., Nikiforov, Y. E., & Carty, S. E. (2022). Clinicopathological features and outcomes of thyroid nodules with EIF1AX mutations. Endocrine-Related Cancer, 1(aop).

Zhang, Q., Li, W., Feng, P., Liu, Y., Chu, B., Zhao, J., ... & Liu, J. (2022). Lnc5926 is essential for early embryonic development in goats through regulation of ZSCAN4 and EIF1AX. Theriogenology, 180, 87-93.

Lv, C., Sun, J., Ye, Y., Lin, Z., Li, H., Liu, Y., ... & Wang, S. (2022). Long noncoding RNA EIF1AX‐AS1 promotes endometrial cancer cell apoptosis by affecting EIF1AX mRNA stabilization. Cancer science, 113(4), 1277.

Li, Y., Guo, L., Ying, S., Feng, G. H., & Zhang, Y. (2020). Transcriptional repression of p21 by EIF1AX promotes the proliferation of breast cancer cells. Cell Proliferation, 53(10), e12903.

Hou, C., Xiao, L., Ren, X., Tang, F., Guo, B., Zeng, W., ... & Yan, N. (2020). Mutations of GNAQ, GNA11, SF3B1, EIF1AX, PLCB4 and CYSLTR in Uveal melanoma in Chinese patients. Ophthalmic research, 63(3), 358-368.

Krishnamoorthy, G. P., Davidson, N. R., Leach, S. D., Zhao, Z., Lowe, S. W., Lee, G., ... & Fagin, J. A. (2019). EIF1AX and RAS Mutations Cooperate to Drive Thyroid Tumorigenesis through ATF4 and c-MYCEIF1AX and RAS Cooperate to Generate mTOR Kinase Dependency0000-0002-5284-9650. Cancer discovery, 9(2), 264-281.

Simões-Pereira, J., Moura, M. M., Marques, I. J., Rito, M., Cabrera, R. A., Leite, V., & Cavaco, B. M. (2019). The role of EIF1AX in thyroid cancer tumourigenesis and progression. Journal of Endocrinological Investigation, 42(3), 313-318.

Alzahrani, A. S., Murugan, A. K., Qasem, E., Alswailem, M. M., AlGhamdi, B., Moria, Y., & Al-Hindi, H. (2019). Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer. Endocrine, 63(1), 94-100.

Topf, M. C., Wang, Z. X., Tuluc, M., & Pribitkin, E. A. (2018). TERT, HRAS, and EIF1AX Mutations in a Patient with Follicular Adenoma. Thyroid, 28(6), 815-817.

Rose, A. M., Luo, R., Radia, U. K., Kalirai, H., Thornton, S., Luthert, P. J., ... & Rose, G. E. (2018). Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis. BMC cancer, 18(1), 1-9.

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