[Gly21]-Beta-Amyloid (1-40), A21G Flemish Mutation

The A21G Flemish variant is associated with familial amyloid disease and has distinct aggregation and vascular-deposition behavior. This Aβ40 form is useful for mutation-dependent assembly comparisons.

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

Mutation identity and Aβ C-terminal length are integral to this reagent. Compare with the sequence-matched wild-type Aβ40 or Aβ42 under identical preparation and aggregation conditions.

1. Selected mutation/amyloid study