WB
Western blot analysis of various lysates using α-Synuclein Rabbit mAb at 1:1000 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Negative control (NC): T-47D Exposure time: 90s.
IHC
Immunohistochemistry analysis of paraffin embedded Rat brain tissue using α-Synuclein Rabbit mAb at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
ICC/IF
Confocal imaging of HEL cells using α Synuclein Rabbit mAb (dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). objective: 100x.
IP
Immunoprecipitation of α-Synuclein in 500 µg extracts from HEL cells using 2 µg α-Synuclein Rabbit mAb. Western blot analysis was performed using α-Synuclein Rabbit mAb at 1:3000 dilution.