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. 1998 Aug 4;95(16):9631–9636. doi: 10.1073/pnas.95.16.9631

Figure 1.

Figure 1

(A) The two-step mating scheme used to produce SOD1G85R, NF-L −/− mice. (B) Immunoblot of 20-μg spinal cord extracts made by using an antibody that recognizes mouse and human SOD1G85R with equal affinity. (C) Parallel Coomassie blue-stained gel demonstrating comparable protein loading. (D and E) Coomassie blue-stained SDS/PAGE gel (D) and immunoblots (E) to measure NF-H and NF-L in 20 μg of sciatic nerve or spinal cord from wild-type mice and heterozygous NF-L and homozygous NF-L knockout mice.