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. 2002 Jan;160(1):101–112. doi: 10.1016/s0002-9440(10)64354-4

Figure 1.

Figure 1.

Characterization of Aβ peptides. A and B: Solutions containing Aβ 42-1 and 1-42 were prepared as described in Materials and Methods and used to coat multispot slides. A: Spots coated with Aβ 42-1 and incubated with Thioflavin S for 1 minute remained unstained implying no fibril formation. B: Spots coated with Aβ 1-42 and incubated with Thioflavin S (Sigma) for 1 minute stained intensely. C: A transmission electron micrograph of negatively stained Aβ 1-42 fibrils (original magnification, ×65,000). D: Nonreducing SDS-PAGE of fAβ 1-42 and 42-1 peptides stained with Coomassie blue (Sigma). The lane containing fAβ 1-42 peptides shows two bands, one at ≅4.2 kd and one at ≅21 kd, whereas the lane containing 42-1 contains a single band at ≅4.2 kd.