[Gly21]-Beta-Amyloid (1-42), Flemish Mutation

The A21G Flemish mutation is associated with familial amyloid disease and changes Aβ assembly and vascular deposition. This Aβ42 form allows direct comparison with the corresponding Aβ40 mutant.

• familial Aβ mutation studies
• amyloid aggregation and oligomerization
• cerebral amyloid angiopathy research
• mutant versus wild-type comparisons

Mutation identity and Aβ length define this reagent. Compare with sequence-matched wild-type Aβ42 or the corresponding Aβ40 mutant under identical preparation conditions.

1. Selected familial amyloid mutation publication