Mouse Anti-DOCK7 Recombinant Antibody (9j45) (V2LY-0425-LY773)

Kapoor, D., Anand, A., Siddiqui, S., & Sharma, S. (2022). A novel pathogenic variant in DOCK 7 gene in an infant with dysmorphism, epileptic encephalopathy and cortical blindness. Clinical Dysmorphology, 31(1), 39-41.

Gao, M., Guo, G., Huang, J., Hou, X., Ham, H., Kim, W., ... & Lou, Z. (2021). DOCK7 protects against replication stress by promoting RPA stability on chromatin. Nucleic acids research, 49(6), 3322-3337.

Haberlandt, E., Valovka, T., Janjic, T., Müller, T., Blatsios, G., Karall, D., & Janecke, A. R. (2021). Characteristic facial features and cortical blindness distinguish the DOCK7‐related epileptic encephalopathy. Molecular Genetics & Genomic Medicine, 9(3), e1607.

Turkdogan, D., Turkyilmaz, A., Gormez, Z., Sager, G., & Ekinci, G. (2019). A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy. Seizure-European Journal of Epilepsy, 66, 12-14.

Kukimoto-Niino, M., Tsuda, K., Ihara, K., Mishima-Tsumagari, C., Honda, K., Ohsawa, N., & Shirouzu, M. (2019). Structural basis for the dual substrate specificity of DOCK7 guanine nucleotide exchange factor. Structure, 27(5), 741-748.

Bai, B., Guo, Y. R., Zhang, Y. H., Jin, C. C., Zhang, J. M., Chen, H., & Zhu, B. S. (2019). Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23. Chinese medical journal, 132(05), 600-603.

Mayer, L., Jasztal, M., Pardo, M., Aguera de Haro, S., Collins, J., Bariana, T. K., ... & Guerrero, J. A. (2018). Nbeal2 interacts with dock7, sec16a, and vac14. Blood, The Journal of the American Society of Hematology, 131(9), 1000-1011.

Li, W. J., Yin, R. X., Cao, X. L., Chen, W. X., Huang, F., & Wu, J. Z. (2018). DOCK7-ANGPTL3 SNPs and their haplotypes with serum lipid levels and the risk of coronary artery disease and ischemic stroke. Lipids in Health and Disease, 17(1), 1-12.

Nakamuta, S., Yang, Y. T., Wang, C. L., Gallo, N. B., Yu, J. R., Tai, Y., & Van Aelst, L. (2017). Dual role for DOCK7 in tangential migration of interneuron precursors in the postnatal forebrain. Journal of Cell Biology, 216(12), 4313-4330.

Le, P. T., Bishop, K. A., Maridas, D. E., Motyl, K. J., Brooks, D. J., Nagano, K., ... & Rosen, C. J. (2017). Spontaneous mutation of Dock7 results in lower trabecular bone mass and impaired periosteal expansion in aged female Misty mice. Bone, 105, 103-114.

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