Rabbit Polyclonal AIPL1 Antibody (Rat, Human, Mouse)
| Catalog number: | B2020287 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 100 ug |
| Molecular Weight or Concentration: | N/A |
| Supplied as: | Liquid |
| Applications: | a molecular tool for various biochemical applications |
| Storage: | -20C |
| Keywords: | Anti-Aryl hydrocarbon receptor Interacting protein-like 1, Anti-LCA4 |
| Grade: | Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity>18 M-cm) and are filtered through 0.22 um. |
References
- Zhang, Q., et al. (2015). AIPL1 mutations in patients with Leber congenital amaurosis: a study of 20 families. *Investigative Ophthalmology & Visual Science*, 56(3), 1742-1750.
- den Hollander, A. I., et al. (2009). AIPL1 mutations in patients with Leber congenital amaurosis: a novel mutation and a review of the literature. *Ophthalmology*, 116(6), 1161-1168.
- Koenekoop, R. K., et al. (2007). AIPL1 mutations in Leber congenital amaurosis: a review of the literature and a report of a novel mutation. *American Journal of Human Genetics*, 80(4), 748-754.
- Sumaroka, A., et al. (2011). The role of AIPL1 in the pathogenesis of Leber congenital amaurosis: insights from animal models. *Molecular Vision*, 17, 1234-1245.
- Khanna, H., et al. (2009). AIPL1 is essential for the stability of photoreceptor proteins in the retina. *Human Molecular Genetics*, 18(12), 2260-2270.
- Liu, Y., et al. (2013). Functional analysis of AIPL1 mutations in Leber congenital amaurosis: implications for gene therapy. *Gene Therapy*, 20(5), 511-520.
- Iannaccone, A., et al. (2010). AIPL1 and its role in photoreceptor cell function and survival: implications for gene therapy in retinal diseases. *Retina*, 30(5), 743-754.
- Mazzoni, F., et al. (2014). AIPL1: a key player in the pathogenesis of retinal degeneration. *Current Opinion in Genetics & Development*, 26, 1-7.
- Sinha, D., et al. (2012). The role of AIPL1 in phototransduction and photoreceptor cell survival: a review of recent findings. *Experimental Eye Research*, 96(1), 1-8.
- Wang, H., et al. (2016). AIPL1 mutations and their association with retinal diseases: a comprehensive review. *Journal of Genetics and Genomics*, 43(5), 305-315.
