NHLH2 Matched Antibody Pair (799) (APMAB-799LY)

Madsen, A. T., & Good, D. J. (2023). In Silico Examination of Single Nucleotide Missense Mutations in NHLH2, a Gene Linked to Infertility and Obesity. International Journal of Molecular Sciences, 24(4), 3193.

Topaloglu, A. K., Simsek, E., Kocher, M. A., Mammadova, J., Bober, E., Kotan, L. D., ... & Good, D. J. (2022). Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans. Human Genetics, 141(2), 295-304.

Kummerfeld, D. M., Skryabin, B. V., Brosius, J., Vakhrushev, S. Y., & Rozhdestvensky, T. S. (2022). Reference genes across nine brain areas of wild type and Prader-Willi Syndrome mice: Assessing differences in Igfbp7, Pcsk1, Nhlh2 and Nlgn3 expression. International Journal of Molecular Sciences, 23(15), 8729.

Katzendorn, O., Peters, I., Dubrowinskaja, N., Moog, J. M., Reese, C., Tezval, H., ... & Serth, J. (2021). DNA methylation in INA, NHLH2, and THBS4 is associated with metastatic disease in renal cell carcinoma. Cancers, 14(1), 39.

Carraro, R. S., Nogueira, G. A., Sidarta-Oliveira, D., Gaspar, R. S., Dragano, N. R., Morari, J., ... & Velloso, L. A. (2021). Arcuate nucleus overexpression of NHLH2 reduces body mass and attenuates obesity-associated anxiety/depression-like behavior. Journal of Neuroscience, 41(48), 10004-10022.

Leon, S., Talbi, R., McCarthy, E. A., Ferrari, K., Fergani, C., Naule, L., ... & Navarro, V. M. (2021). Sex-specific pubertal and metabolic regulation of Kiss1 neurons via Nhlh2. Elife, 10, e69765.

Kocher, M. A., Huang, F. W., Le, E., & Good, D. J. (2021). Snord116 post-transcriptionally increases Nhlh2 mRNA stability: implications for human Prader-Willi syndrome. Human Molecular Genetics, 30(12), 1101-1110.

Hadziselimovic, F., Verkauskas, G., & Stadler, M. B. (2021). Molecular clues in the regulation of mini‐puberty involve neuronal DNA binding transcription factor NHLH2. Basic and clinical andrology, 31, 1-13.

Afshar, H., Adelirad, F., Kowsari, A., Kalhor, N., Delbari, A., Najafipour, R., ... & Ohadi, M. (2020). Natural selection at the NHLH2 core promoter exceptionally long CA-repeat in human and disease-only genotypes in late-onset neurocognitive disorder. Gerontology, 66(5), 514-522.

Li, W., Guo, B., Tao, K., Li, F., Liu, Z., Yao, H., ... & Liu, X. (2019). Inhibition of SIRT1 in hippocampal CA1 ameliorates PTSD-like behaviors in mice by protections of neuronal plasticity and serotonin homeostasis via NHLH2/MAO-A pathway. Biochemical and Biophysical Research Communications, 518(2), 344-350.

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

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Isotype control