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- Product number
- ABIN394451 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Aryl Hydrocarbon Receptor Interacting Protein-Like 1 (AIPL1) (AA 1-385) antibody
- Antibody type
- Monoclonal
- Description
- This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 1-385
- Isotype
- IgG
- Antibody clone number
- 1E1
- Vial size
- 100 μg
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Submitted references Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosis.
The Leber congenital amaurosis protein, AIPL1, is needed for the viability and functioning of cone photoreceptor cells.
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India.
The Leber congenital amaurosis protein AIPL1 functions as part of a chaperone heterocomplex.
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.
Pasadhika S, Fishman GA, Stone EM, Lindeman M, Zelkha R, Lopez I, Koenekoop RK, Shahidi M
Investigative ophthalmology & visual science 2010 May;51(5):2608-14
Investigative ophthalmology & visual science 2010 May;51(5):2608-14
The Leber congenital amaurosis protein, AIPL1, is needed for the viability and functioning of cone photoreceptor cells.
Kirschman LT, Kolandaivelu S, Frederick JM, Dang L, Goldberg AF, Baehr W, Ramamurthy V
Human molecular genetics 2010 Mar 15;19(6):1076-87
Human molecular genetics 2010 Mar 15;19(6):1076-87
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India.
Sundaresan P, Vijayalakshmi P, Thompson S, Ko AC, Fingert JH, Stone EM
Molecular vision 2009 Sep 4;15:1781-7
Molecular vision 2009 Sep 4;15:1781-7
The Leber congenital amaurosis protein AIPL1 functions as part of a chaperone heterocomplex.
Hidalgo-de-Quintana J, Evans RJ, Cheetham ME, van der Spuy J
Investigative ophthalmology & visual science 2008 Jul;49(7):2878-87
Investigative ophthalmology & visual science 2008 Jul;49(7):2878-87
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.
Booij JC, Florijn RJ, ten Brink JB, Loves W, Meire F, van Schooneveld MJ, de Jong PT, Bergen AA
Journal of medical genetics 2005 Nov;42(11):e67
Journal of medical genetics 2005 Nov;42(11):e67
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Supportive validation
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Supportive validation
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