Mouse Anti-ERCC8 Recombinant Antibody (E1738) (V2LY-0825-LY678)

Mamoor, S. (2022). A single nucleotide variant on chromosome 5 residing within ERCC8 distinguishes patients with basal-like human breast cancer.

Duong, N. T., Dinh, T. H., Möhl, B. S., Hintze, S., Ha, D. T. T., Ngoc, N. D., ... & Meinke, P. (2022). Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants. Aging (Albany NY), 14(13), 5299.

Gauhar, Z., Tejwani, L., Abdullah, U., Saeed, S., Shafique, S., Badshah, M., ... & Raja, G. K. (2022). A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family. Cells, 11(19), 3090.

Sui, X., Tang, X., Wu, X., & Liu, Y. (2022). Identification of ERCC8 as a novel cisplatin-resistant gene in esophageal cancer based on genome-scale CRISPR/Cas9 screening. Biochemical and Biophysical Research Communications, 593, 84-92.

Yousefipour, F., & Mahjoobi, F. (2021). Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran. Clinica Chimica Acta, 523, 65-71.

Chen, J., Li, L., Sun, L., Yuan, Y., & Jing, J. (2021). Associations of individual and joint expressions of ERCC6 and ERCC8 with clinicopathological parameters and prognosis of gastric cancer. PeerJ, 9, e11791.

Moslehi, R., Tsao, H. S., Zeinomar, N., Stagnar, C., Fitzpatrick, S., & Dzutsev, A. (2020). Integrative genomic analysis implicates ERCC6 and its interaction with ERCC8 in susceptibility to breast cancer. Scientific reports, 10(1), 1-13.

Zhang, D., Dai, L., Zhou, Z., Hu, J., Bai, Y., & Guo, H. (2019). Homozygosity mapping and whole exome sequencing reveal a novel ERCC8 mutation in a Chinese consanguineous family with unique cerebellar ataxia. Clinica Chimica Acta, 494, 64-70.

Lu, X., Chen, F., Liu, X., Yuan, D., Zi, Y., He, X., & Zhu, D. (2018). Detection and clinical significance of DNA repair gene ERCC8 tag SNPs in gastric cancer. The Turkish Journal of Gastroenterology, 29(4), 392.

Chebly, A., Corbani, S., Abou Ghoch, J., Mehawej, C., Megarbane, A., & Chouery, E. (2018). First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene. BMC medical genetics, 19(1), 1-7.

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