Mouse Anti-L2HGDH Recombinant Antibody (A852) (CBMAB-AP11298LY)

Muzammal, M., Ali, M. Z., Brugger, B., Blatterer, J., Ahmad, S., Taj, S., ... & Windpassinger, C. (2022). A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani family. Metabolic Brain Disease, 1-10.

Christen, M., Janzen, N., Fraser, A., Sewell, A. C., Jagannathan, V., Guevar, J., ... & Sanchez-Masian, D. (2021). L2HGDH missense variant in a cat with L-2-hydroxyglutaric aciduria. Genes, 12(5), 682.

Ullah, M. I., Nasir, A., Ahmad, A., Harlalka, G. V., Ahmad, W., Hassan, M. J., ... & Chioza, B. A. (2018). Identification of novel L2HGDH mutation in a large consanguineous Pakistani family-a case report. BMC medical genetics, 19, 1-5.

Zhang, Y., Wang, C., Yang, K., Wang, S., Tian, G., & Chen, Y. (2018). A novel compound heterozygous mutation of the L2HGDH gene in a Chinese boy with L-2-hydroxyglutaric aciduria: case report and literature review. Neurological Sciences, 39, 1697-1703.

Peng, W., Ma, X. W., Yang, X., Zhang, W. Q., Yan, L., Wang, Y. X., ... & Feng, Z. C. (2018). Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria. BMC Medical Genetics, 19(1), 1-5.

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