Rabbit Anti-NAPB Recombinant Antibody (CBXS-1395) (CBMAB-S4253-CQ)

Ali, G., Shin, K. C., Habbab, W., Alkhadairi, G., AbdelAleem, A., AlShaban, F. A., ... & Stanton, L. W. (2023). Characterization of a loss-of-function NSF attachment protein beta mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived and CRISPR-corrected induced pluripotent stem cell lines. Frontiers in Neuroscience, 17.

Mignon‐Ravix, C., Riccardi, F., Daquin, G., Cacciagli, P., Lamoureux‐Toth, S., Villard, L., ... & Molinari, F. (2023). NAPB and developmental and epileptic encephalopathy: description of the electro‐clinical profile associated to a novel pathogenic variant. Epilepsia.

AbdelAleem, A., Haddad, N., Al-Ettribi, G., Crunk, A., & Elsotouhy, A. (2023). Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB. neurogenetics, 24(2), 103-112.

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