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- Product number
- ABIN396373 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Aminoacylase 1 (ACY1) (AA 1-409) 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 1-409
- Isotype
- IgG
- Antibody clone number
- 4F1-B7
- 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 Probing the acyl-binding pocket of aminoacylase-1.
The amidase activity of human tissue kallikrein is significantly lower in the urine of patients with systolic heart failure.
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism.
Towards a proteome-scale map of the human protein-protein interaction network.
Aminoacylase I deficiency: a novel inborn error of metabolism.
Lindner HA, Alary A, Wilke M, Sulea T
Biochemistry 2008 Apr 8;47(14):4266-75
Biochemistry 2008 Apr 8;47(14):4266-75
The amidase activity of human tissue kallikrein is significantly lower in the urine of patients with systolic heart failure.
Figueiredo EL, Garcia Leão FV, De Oliveira LV, Moreira Mda C, De Souza Figueiredo AF
Journal of cardiac failure 2006 Oct;12(8):653-8
Journal of cardiac failure 2006 Oct;12(8):653-8
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism.
Sass JO, Mohr V, Olbrich H, Engelke U, Horvath J, Fliegauf M, Loges NT, Schweitzer-Krantz S, Moebus R, Weiler P, Kispert A, Superti-Furga A, Wevers RA, Omran H
American journal of human genetics 2006 Mar;78(3):401-9
American journal of human genetics 2006 Mar;78(3):401-9
Towards a proteome-scale map of the human protein-protein interaction network.
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M
Nature 2005 Oct 20;437(7062):1173-8
Nature 2005 Oct 20;437(7062):1173-8
Aminoacylase I deficiency: a novel inborn error of metabolism.
Van Coster RN, Gerlo EA, Giardina TG, Engelke UF, Smet JE, De Praeter CM, Meersschaut VA, De Meirleir LJ, Seneca SH, Devreese B, Leroy JG, Herga S, Perrier JP, Wevers RA, Lissens W
Biochemical and biophysical research communications 2005 Dec 23;338(3):1322-6
Biochemical and biophysical research communications 2005 Dec 23;338(3):1322-6
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Supportive validation
- Submitted by
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