[Gly21]-beta-Amyloid (1-40), A21G, Flemish Mutation - 0.5 mg
- Cat.Number : AS-62150
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Several mutations in the beta amyloid precursor gene cause autosomal dominant Alzheimer's Disease in a number of kindreds. Amond them, the A21G Flemish mutation is unique as it shows a low tendency to aggregation, while deposits progressively appear in the vessel walls. In addition, the brain deposits are prefereably composed of A-beta 1-40 rather than A beta 1-42, in opposition to the other familial AD.
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References
Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation
Neurol . 2004 Nov 09 ; 63(9) 1613 | DOI : https://doi.org/10.1212/01.WNL.0000142965.10778.C7
- W. Brooks
- et al
Impact of the Mutation A21G (Flemish Variant) on Alzheimer’s β-Amyloid Dimers by Molecular Dynamics Simulations
Biophys J . 2006 Nov 15 ; 91(10) 3829 | DOI : https://doi.org/10.1529/biophysj.106.090993
- A. Huet
- P. Derreumaux
Pathogenic Effects of D23N Iowa Mutant Amyloid β-Protein
J Biol Chem . 2001 Aug 01 ; 276(35) 32860 | DOI : https://doi.org/10.1074/jbc.M104135200
- W. Van Nostrand
- et al