Rabbit Anti-NPHS1 Recombinant Antibody (9H482) (CBMAB-N3129-WJ)

Xie, D., Wu, J., Zhang, W., Jin, T., Wu, P., An, B., & Huang, S. (2023). A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report. Medicine, 102(7).

Espinosa, L. G., Santoveña, A. Z., Blanco, J. N., Alvariño, M. G., Feito, J. B., & Hijosa, M. M. (2022). Spontaneous remission in a child with an NPHS1-based congenital nephrotic syndrome. Clinical Kidney Journal, 15(10), 1969-1970.

Thomas, M. M., Ahmed, H. M., El-Dessouky, S. H., Ramadan, A., Botrous, O. E., & Abdel-Hamid, M. S. (2022). Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect. Molecular Genetics and Genomics, 297(3), 689-698.

Khaliq, O. P., Konoshita, T., Moodley, J., & Naicker, T. (2021). The association of NPHS1 and ACNT4 gene polymorphisms with pre-eclampsia. European Journal of Obstetrics & Gynecology and Reproductive Biology, 266, 9-14.

Rong, L., Chen, L., Rao, J., Shen, Q., Li, G., Liu, J., ... & Xu, H. (2021). Genetic Variations and Clinical Features of NPHS1-Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study. Frontiers in Medicine, 8, 771227.

Jia, X., Yamamura, T., Gbadegesin, R., McNulty, M. T., Song, K., Hitomi, Y., ... & Weaver, D. J. (2020). Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. Kidney international, 98(5), 1308-1322.

Amr, K., El-Bassyouni, H. T., Rabie, E., Selim, A., Zaki, M. E., Abd Alazem, E. A., ... & Salah, D. M. (2020). A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome. Gene Reports, 20, 100722.

Zhuo, L., Huang, L., Yang, Z., Li, G., & Wang, L. (2019). A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis. BMC medical genetics, 20, 1-8.

Thi Kim Lien, N., Van Dem, P., Thu Huong, N., Minh Dien, T., Thi Thu Thuy, T., Van Tung, N., ... & Thi Quynh Huong, N. (2019). The role of p. Ser1105Ser (in NPHS1 gene) and p. Arg548Leu (in PLCE1 gene) with disease status of Vietnamese patients with congenital nephrotic syndrome: benign or pathogenic?. Medicina, 55(4), 102.

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