Rabbit Anti-GTF2I Recombinant Antibody (EG1465) (CBMAB-EN1751-LY)

Pan, Y., Iejima, D., Nakayama, M., Suga, A., Noda, T., Kaur, I., ... & Iwata, T. (2021). Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro. Journal of Biological Chemistry, 296.

Lee, J., Rho, J. H., Roehrl, M. H., & Wang, J. Y. (2021). Dermatan sulfate is a potential regulator of IgH via interactions with pre-BCR, GTF2I, and BiP ER complex in pre-B lymphoblasts. Frontiers in immunology, 12, 680212.

Liu, C., Yan, S., Chen, H., Wu, Z., Li, L., Cheng, L., ... & Li, Y. (2021). Association of GTF2I, NFKB1, and TYK2 regional polymorphisms with systemic sclerosis in a Chinese Han population. Frontiers in Immunology, 12, 640083.

Shimoyama, S., Nakagawa, I., Jiang, J. J., Matsumoto, I., Chiorini, J. A., Hasegawa, Y., ... & Murakami, M. (2021). Sjögren’s syndrome-associated SNPs increase GTF2I expression in salivary gland cells to enhance inflammation development. International immunology, 33(8), 423-434.

Cavallo, F., Troglio, F., Fagà, G., Fancelli, D., Shyti, R., Trattaro, S., ... & Testa, G. (2020). High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11. 23 microduplication autism spectrum disorder patient-derived cortical neurons. Molecular autism, 11(1), 1-18.

Kim, I. K., Rao, G., Zhao, X., Fan, R., Avantaggiati, M. L., Wang, Y., ... & Giaccone, G. (2020). Mutant GTF2I induces cell transformation and metabolic alterations in thymic epithelial cells. Cell Death & Differentiation, 27(7), 2263-2279.

Higuchi, R., Goto, T., Hirotsu, Y., Yokoyama, Y., Nakagomi, T., Otake, S., ... & Omata, M. (2020). Primary driver mutations in GTF2I specific to the development of thymomas. Cancers, 12(8), 2032.

Barak, B., Zhang, Z., Liu, Y., Nir, A., Trangle, S. S., Ennis, M., ... & Feng, G. (2019). Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug. Nature neuroscience, 22(5), 700-708.

Kopp, N., McCullough, K., Maloney, S. E., & Dougherty, J. D. (2019). Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models. Human molecular genetics, 28(20), 3443-3465.

Chailangkarn, T., Noree, C., & Muotri, A. R. (2018). The contribution of GTF2I haploinsufficiency to Williams syndrome. Molecular and cellular probes, 40, 45-51.

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