Anti-PNPLA1 Antibody Picoband® (ABIN7600045). Tested in WB, ELISA applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
纯化方法
Immunogen affinity purified.
免疫原
E.coli-derived human PNPLA1 recombinant protein (Position: K141-D496). Human PNPLA1 shares 51.5% amino acid (aa) sequence identity with mouse PNPLA1.
Western blot, 0.25-0.5 μg/mL, Human ELISA, 0.1-0.5 μg/mL, - 1. Ahmad, F., Ansar, M., Mehmood, S., Izoduwa, A., Lee, K., Nasir, A., Abrar, M., Mehmood, S., Ullah, A., Aziz, A., University of Washington Center for Mendelian Genomics, Smith, J. D., Shendure, J., Bamshad, M. J., Nicekrson, D. A., Santos-Cortez, R. L. P., Leal, S. M., Ahmad, W. A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families. J. Europ. Acad. Derm. Venereol. 30: e210-e213, 2016. Note: Electronic Article. 2. Boyden, L. M., Craiglow, B. G., Hu, R. H., Zhou, J., Browning, J., Eishenfield, L., Lim, Y. L., Luu, M., Randolph, L. M., Ginarte, M., Fachal, L., Rodriguez-Pazos, L., and 10 others. Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation. Brit. J. Derm. 177: 319-322, 2017. 3. Fachal, L., Rodriguez-Pazos, L., Ginarte, M., Carracedo, A., Toribio, J., Vega, A. Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis. (Letter) Brit. J. Derm. 170: 980-982, 2014.
限制
仅限研究用
状态
Lyophilized
溶解方式
Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.