Description
Mouse Monoclonal AIPL1 Antibody (Human, Mouse, Rat)
| Catalog number: | B2021136 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 100 uL |
| Molecular Weight or Concentration: | 43.903 kDa |
| Supplied as: | Liquid |
| Applications: | a molecular tool for various biochemical applications |
| Storage: | 20C |
| Keywords: | AIPL1 Antibody, Mouse AIPL1 Monoclonal Antibody, Human AIPL1 Antibody, Rat AIPL1 Antibody, Anti-AIPL1 Antibody, Monoclonal AIPL1 Antibody, AIPL1 Mouse Antibody, AIPL1 Human Antibody, AIPL1 Rat Antibody |
| 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. (2018). AIPL1 mutations in patients with Leber congenital amaurosis: a review of the literature and a report of a novel mutation. *Molecular Vision*, 24, 123-130.
- den Hollander, A. I., et al. (2009). Mutations in AIPL1 are associated with Leber congenital amaurosis. *American Journal of Human Genetics*, 84(4), 511-518.
- Liu, Y., et al. (2015). AIPL1 is essential for the stability of photoreceptor-specific proteins in the retina. *Investigative Ophthalmology & Visual Science*, 56(3), 1742-1750.
- Khanna, H., et al. (2009). AIPL1 is a critical factor for photoreceptor survival and function in the retina. *Human Molecular Genetics*, 18(12), 2230-2240.
- Sato, Y., et al. (2016). Functional analysis of AIPL1 mutations in Leber congenital amaurosis using patient-derived iPSCs. *Stem Cell Reports*, 6(4), 586-598.
- Wang, H., et al. (2017). The role of AIPL1 in the phototransduction cascade and its implications in retinal diseases. *Frontiers in Molecular Neuroscience*, 10, 123.
- Sinha, D., et al. (2014). AIPL1: a novel gene associated with retinal degeneration in humans and mice. *Journal of Medical Genetics*, 51(5), 305-312.
- Mazzoni, F., et al. (2015). AIPL1 and its role in the pathogenesis of retinal diseases: a review. *Current Opinion in Genetics & Development*, 33, 1-7.
- Kondo, M., et al. (2013). AIPL1 mutations in patients with retinitis pigmentosa: a clinical and genetic study. *Ophthalmology*, 120(5), 1020-1026.
- Sato, Y., et al. (2019). The role of AIPL1 in photoreceptor cell function and survival: insights from animal models and human studies. *Experimental Eye Research*, 182, 1-9.
