WB
Western blot analysis of lysates from wild type (WT) and Abhd6 knockout (KO) Mouse brain using [KOValidated] Abhd6 Rabbit mAb at 1:6000 dilution incubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 20s.
WB
Western blot analysis of various lysates using [KO Validated] Abhd6 Rabbit mAb at 1:6000dilution incubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L)at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 20s.
WB
Western blot analysis of lysates from RPMI 8226 cells using [KO Validated] Abhd6 Rabbit mAb at1:6000 dilution incubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 60s.
IHC
Immunohistochemistry analysis of paraffinembedded Rat brain tissue using [KOValidated] Abhd6 Rabbit mAb at adilution of 1:200 (40x lens). High pressureantigen retrieval performed with 0.01M TrisEDTA Buffer (pH 9.0) prior to IHC staining.
IF-F
Confocal imaging of frozen sections Mousebrain tissue using [KO Validated] Abhd6Rabbit mAb (dilution 1:200)followed by a further incubation with Cy3Goat Anti-Rabbit IgG (H+L) (dilution1:500) (Red). DAPI was used for nuclearstaining (Blue). Microwave antigen retrievalperformed with 0.01M Citrate Buffer (pH 6.0)prior to IF staining. Objective: 40x.